PMID-sentid	Pub_year	Sent_text	comp_official_name	comp_offset	protein_name	organism	prot_offset
7688730-2	1993	Countertrypin is a 53-kDa glycoprotein having about 30% carbohydrate, and did not cross-react immunologically with either mouse alpha 1-antiproteinase (also called alpha 1-proteinase inhibitor or alpha 1-antitrypsin) or contrapsin.	Carbohydrates	56-68	alpha-2-HS-glycoprotein	Mus musculus	0-13
8866020-5	1996	In the present study, cDNA encoding countertrypin was isolated and sequenced, and evidence is presented, based on the site-directed mutagenesis, that lysine-231 in the second cystatin domain is the P1 site for trypsin inhibition.	Lysine	150-156	alpha-2-HS-glycoprotein	Mus musculus	36-49
11374033-7	2001	A mineral binding structure is proposed for domain D1 of AHSG suggesting that the proposed EF-hand motif for calcium binding does not exist in AHSG.	Calcium	109-116	alpha-2-HS-glycoprotein	Mus musculus	57-61
31077645-0	2019	Hepatic upregulation of fetuin-A mediates acetaminophen-induced liver injury through activation of TLR4 in mice.	Acetaminophen	42-55	alpha-2-HS-glycoprotein	Mus musculus	24-32
33033766-0	2020	Combination of Pancreastatin inhibitor PSTi8 with metformin inhibits Fetuin-A in type 2 diabetic mice.	Metformin	50-59	alpha-2-HS-glycoprotein	Mus musculus	69-77
31077645-6	2019	Treatment with APAP increased the expression and serum levels of fetuin-A in mice.	Acetaminophen	15-19	alpha-2-HS-glycoprotein	Mus musculus	65-73
31077645-11	2019	Our results indicate that a strategy based on the antagonism of fetuin-A may be a novel therapeutic approach to the treatment of acetaminophen-induced acute liver failure.	Acetaminophen	129-142	alpha-2-HS-glycoprotein	Mus musculus	64-72
34224584-3	2022	Recently, we have also reported that beta-cells secrete fetuin-A on stimulation by palmitate causing beta-cell dysfunction.	Palmitates	83-92	alpha-2-HS-glycoprotein	Mus musculus	56-64
34224584-8	2022	Knockdown of fetuin-A gene partially inhibited palmitate inflicted apoptosis in MIN6 by 1.83 +- 0.25 times, however, fetuin-A when added in the medium caused re-emergence of apoptosis.	Palmitates	47-56	alpha-2-HS-glycoprotein	Mus musculus	13-21
34224584-9	2022	Notably, apoptosis induced by palmitate conditioned media from MIN6, 3T3L1, and HepG2, was partially inhibited in fetuin-A KD MIN6.	Palmitates	30-39	alpha-2-HS-glycoprotein	Mus musculus	114-122
34374422-7	2021	In the blood, calcium-phosphate precipitated upon increase in the blood phosphate concentration is adsorbed by serum protein fetuin-A to form colloidal nanoparticles called calciprotein particles (CPPs).	calcium phosphate	14-31	alpha-2-HS-glycoprotein	Mus musculus	125-133
34374422-7	2021	In the blood, calcium-phosphate precipitated upon increase in the blood phosphate concentration is adsorbed by serum protein fetuin-A to form colloidal nanoparticles called calciprotein particles (CPPs).	Phosphates	72-81	alpha-2-HS-glycoprotein	Mus musculus	125-133
32001068-4	2020	Calciprotein particles are nanoparticles of calcium-phosphate precipitates bound to serum protein fetuin-A and are generated spontaneously in solution containing calcium, phosphate, and fetuin-A to be dispersed as colloids.	calcium phosphate	44-61	alpha-2-HS-glycoprotein	Mus musculus	98-106
33182564-7	2020	AE at 500 mg/kg downregulated the PPAR-gamma, SREBP-1c, and fetuin-A mRNA in the liver and upregulated the PPAR-alpha mRNA in white adipose tissue, suggesting that the hypoglycemic effects could be associated with the expression of genes involved in de novo lipogenesis.	ae	0-2	alpha-2-HS-glycoprotein	Mus musculus	60-68
33989718-2	2021	Recently we have reported that MIN6 cells (mouse insulinoma cells) secrete fetuin-A on stimulation by palmitate that aggravates beta-cell dysfunction, but the mechanism involve in-vivo has not been demonstrated and thus remained unclear.	Palmitates	102-111	alpha-2-HS-glycoprotein	Mus musculus	75-83
33989718-5	2021	Further treatment of islets with palmitate raised fetuin-A expression by ~2.8 folds and cut down insulin secretion by ~1.4 folds.	Palmitates	33-42	alpha-2-HS-glycoprotein	Mus musculus	50-58
33989718-7	2021	Altogether this study demonstrated that blocking TLR4, fetuin-A and NF-kappaB protect pancreatic beta-cells from the negative effects of free fatty acid and fetuin-A and restore insulin secretion.	Fatty Acids, Nonesterified	137-152	alpha-2-HS-glycoprotein	Mus musculus	55-63
33028781-8	2021	In the blood, calcium-phosphate crystals are adsorbed by serum protein fetuin-A and prevented from growing into large precipitates.	calcium phosphate	14-31	alpha-2-HS-glycoprotein	Mus musculus	71-79
32001068-4	2020	Calciprotein particles are nanoparticles of calcium-phosphate precipitates bound to serum protein fetuin-A and are generated spontaneously in solution containing calcium, phosphate, and fetuin-A to be dispersed as colloids.	Calcium	44-51	alpha-2-HS-glycoprotein	Mus musculus	98-106
32001068-4	2020	Calciprotein particles are nanoparticles of calcium-phosphate precipitates bound to serum protein fetuin-A and are generated spontaneously in solution containing calcium, phosphate, and fetuin-A to be dispersed as colloids.	Phosphates	52-61	alpha-2-HS-glycoprotein	Mus musculus	98-106
31203904-4	2019	However, recent evidence indicates that fetuin-A can form nucleation seeds or nidi that grow in size through ion sedimentation to become larger amorphous nanoparticles in the presence of excess calcium and apatite ions.	Calcium	194-201	alpha-2-HS-glycoprotein	Mus musculus	40-48
32074140-9	2020	We show that pathological ectopic calcification in fetuin-A deficient DBA/2 mice is caused by a compound deficiency of three major extracellular and systemic inhibitors of calcification, namely fetuin-A, magnesium, and pyrophosphate.	Magnesium	204-213	alpha-2-HS-glycoprotein	Mus musculus	51-59
32074140-9	2020	We show that pathological ectopic calcification in fetuin-A deficient DBA/2 mice is caused by a compound deficiency of three major extracellular and systemic inhibitors of calcification, namely fetuin-A, magnesium, and pyrophosphate.	Diphosphates	219-232	alpha-2-HS-glycoprotein	Mus musculus	51-59
31203904-7	2019	In addition, calcium phosphate nanocrystals that contain fetuin-A are pro-inflammatory to macrophages and promote vascular smooth muscle cell mineralization, potentiating a vicious cycle of inflammation and calcification.	calcium phosphate	13-30	alpha-2-HS-glycoprotein	Mus musculus	57-65
30679396-2	2019	In the blood, phosphorus exists in the form of phosphate ions and colloidal particles composed of solid-phase calcium-phosphate and serum protein fetuin-A, which are termed calciprotein particles(CPP).	Phosphorus	14-24	alpha-2-HS-glycoprotein	Mus musculus	146-154
30788050-12	2019	NR upregulated anti-inflammatory molecule adiponectin, and, tended to down-regulate hepatokine fetuin-A in PA-treated hepatocytes, suggesting its inverse regulation on these cytokines.	Palmitic Acid	107-109	alpha-2-HS-glycoprotein	Mus musculus	95-103
30713844-7	2018	One such example is Fetuin-A, which is mainly produced in the liver and which forms calciprotein particles (CPPs), inhibiting growth of calcium-phosphate crystals in the blood and thereby preventing their soft tissue deposition.	calcium phosphate	136-153	alpha-2-HS-glycoprotein	Mus musculus	20-28
29088242-2	2017	Due to its high affinity for calcium phosphate, fetuin-A is highly abundant in mineralized bone matrix.	calcium phosphate	29-46	alpha-2-HS-glycoprotein	Mus musculus	48-56
29607540-4	2018	The aim of this study was to determine whether melatonin improves hepatic insulin resistance and hepatic steatosis in a FETUA-dependent manner.	Melatonin	47-56	alpha-2-HS-glycoprotein	Mus musculus	120-125
29607540-10	2018	FETUA expression and ER stress markers in the liver and serum of HFD mice were decreased by melatonin treatment.	Melatonin	92-101	alpha-2-HS-glycoprotein	Mus musculus	0-5
29607540-11	2018	In conclusion, melatonin can improve hepatic insulin resistance and hepatic steatosis through reduction in ER stress and the resultant AHSG expression.	Melatonin	15-24	alpha-2-HS-glycoprotein	Mus musculus	135-139
29763604-7	2018	Since MCP1 and FetA drive macrophage to inflamed adipose tissue and IFNgamma promotes M2 to M1 transformation, both recruitment and M1 induced inflammation were found to be significantly repressed by dmp.	Unithiol	200-203	alpha-2-HS-glycoprotein	Mus musculus	15-19
29763604-8	2018	In addressing the question about how dmp induced excess SIRT1 could reduce MCP1, FetA and IFNgamma levels, we found that it was due to the inactivation of NFkappaB because of its deacetylation by SIRT1.	Unithiol	37-40	alpha-2-HS-glycoprotein	Mus musculus	81-85
25098735-12	2014	A significant reduction in the serum biomarkers like Plasminogen activator inhibitor-1 (PAI-1), interleukin 6 (IL-6) and Fetuin-A with CNX-010-49 treatment was observed indicating a potential to modulate processes implicated in cardiovascular benefits.	cnx-010	135-142	alpha-2-HS-glycoprotein	Mus musculus	121-129
25205713-6	2015	Fetuin-A is a liver-derived plasma protein with multiple functions, which is proteolytically processed to yield a disulfide-linked two-chain form.	Disulfides	114-123	alpha-2-HS-glycoprotein	Mus musculus	0-8
25205713-9	2015	Arg and Lys residues located within the 40 residue spanning connecting peptide of fetuin-A were identified as cleavage sites for matriptase-2.	Arginine	0-3	alpha-2-HS-glycoprotein	Mus musculus	82-90
25205713-9	2015	Arg and Lys residues located within the 40 residue spanning connecting peptide of fetuin-A were identified as cleavage sites for matriptase-2.	Lysine	8-11	alpha-2-HS-glycoprotein	Mus musculus	82-90
25205713-12	2015	These findings implicate a role of fetuin-A in iron homeostasis and provide new insights into the mechanism of how matriptase-2 might modulate hepcidin expression.	Iron	47-51	alpha-2-HS-glycoprotein	Mus musculus	35-43
28797566-0	2017	Palmitate induced Fetuin-A secretion from pancreatic beta-cells adversely affects its function and elicits inflammation.	Palmitates	0-9	alpha-2-HS-glycoprotein	Mus musculus	18-26
28797566-6	2017	Fatty acid induces the FetA gene and protein expression in the pancreatic beta-cells via TLR4 and over-expression of NF-kappaB.	Fatty Acids	0-10	alpha-2-HS-glycoprotein	Mus musculus	23-27
28797566-8	2017	These results suggest that NF-kappaB mediates palmitate stimulated FetA secretion from the pancreatic beta-cells.	Palmitates	46-55	alpha-2-HS-glycoprotein	Mus musculus	67-71
28898202-2	2017	Studies in diet-induced obesity have characterized the role of Fetuin A (Fet A) in Free Fatty Acids (FFA)-mediated TLR4 activation and adipose tissue inflammation.	Fatty Acids, Nonesterified	83-99	alpha-2-HS-glycoprotein	Mus musculus	63-71
28898202-2	2017	Studies in diet-induced obesity have characterized the role of Fetuin A (Fet A) in Free Fatty Acids (FFA)-mediated TLR4 activation and adipose tissue inflammation.	Fatty Acids, Nonesterified	83-99	alpha-2-HS-glycoprotein	Mus musculus	73-78
26307633-7	2016	As a result, acetazolamide treatment of kl/kl mice partially reversed the growth deficit, tripled the life span, almost completely reversed the calcifications in trachea, lung, kidney, stomach, intestine, and vascular tissues, the excessive aortic alkaline phosphatase mRNA levels and the plasma concentrations of osteoprotegerin, osteopontin as well as fetuin-A, without significantly decreasing FGF23, 1,25(OH)2D3, Ca(2+), and phosphate plasma concentrations.	Acetazolamide	13-26	alpha-2-HS-glycoprotein	Mus musculus	354-362
26282595-0	2015	Involvement of resveratrol in crosstalk between adipokine adiponectin and hepatokine fetuin-A in vivo and in vitro.	Resveratrol	15-26	alpha-2-HS-glycoprotein	Mus musculus	85-93
26282595-3	2015	This study investigated the involvement of resveratrol (RSV) in the crosstalk between adipokine adiponectin and hepatokine fetuin-A.	Resveratrol	43-54	alpha-2-HS-glycoprotein	Mus musculus	123-131
26282595-3	2015	This study investigated the involvement of resveratrol (RSV) in the crosstalk between adipokine adiponectin and hepatokine fetuin-A.	Resveratrol	56-59	alpha-2-HS-glycoprotein	Mus musculus	123-131
26282595-10	2015	The four-week RSV treatment resulted in increased serum adiponectin and decreased serum fetuin-A in diet-induced obesity mice.	Resveratrol	14-17	alpha-2-HS-glycoprotein	Mus musculus	88-96
26282595-13	2015	RSV lowered fetuin-A and NF-kappaB, and increased liver AMPK.	Resveratrol	0-3	alpha-2-HS-glycoprotein	Mus musculus	12-20
26282595-14	2015	These results demonstrate the crosstalk between adiponectin and fetuin-A, and suggest that RSV may be involved in adipose tissue and liver crosstalk through the interaction between adiponectin and fetuin-A.	Resveratrol	91-94	alpha-2-HS-glycoprotein	Mus musculus	197-205
23577176-1	2013	The formation of fetuin-A-containing calciprotein particles (CPP) may facilitate the clearance of calcium phosphate nanocrystals from the extracellular fluid.	calcium phosphate	98-115	alpha-2-HS-glycoprotein	Mus musculus	17-25
24604240-0	2014	Intraperitoneal administration of fetuin-A attenuates D-galactosamine/lipopolysaccharide-induced liver failure in mouse.	Galactosamine	54-69	alpha-2-HS-glycoprotein	Mus musculus	34-42
24604240-2	2014	AIMS: The purpose of this study was to investigate the effects of fetuin-A on D-galactosamine/lipopolysaccharide (D-GalN/LPS)-induced liver failure in mice.	Galactosamine	78-93	alpha-2-HS-glycoprotein	Mus musculus	66-74
24551137-8	2014	Finally, oral administration of pioglitazone to mice for 8 weeks resulted in suppression of hepatic fetuin-A mRNA.	Pioglitazone	32-44	alpha-2-HS-glycoprotein	Mus musculus	100-108
23277412-10	2013	We posit that the absence of fetuin-A in the growth plate causes simultaneous lack of calcification inhibition and excess lipid hormone signaling, leading to premature growth plate mineralization and shortened long bones.	lipid hormone	122-135	alpha-2-HS-glycoprotein	Mus musculus	29-37
23765754-13	2013	Fetuin A was found to be positively correlated with HOMA-IR (r:0,40, P<0.05) and negatively correlated with 8-hydroxydeoxyguanosine (r:-0,52, P<0.01).	8-ohdg	111-134	alpha-2-HS-glycoprotein	Mus musculus	0-8
23765754-15	2013	In conclusion, serum level of fetuin A is high in morbidly obese subjects and is negatively associated with 8-hydroxydeoxyguanosine level in peripheral circulation.	8-ohdg	108-131	alpha-2-HS-glycoprotein	Mus musculus	30-38
23341496-8	2013	Furthermore, administration of GW-9508 decreased the hepatic expression of fetuin-A in HFD mice significantly and regulated high-glucose- or palmitate-induced fetuin-A expression to increase insulin sensitivity through a GPR40/PLC/PKC pathway in HepG2 cells.	GW9508	31-38	alpha-2-HS-glycoprotein	Mus musculus	75-83
23341496-8	2013	Furthermore, administration of GW-9508 decreased the hepatic expression of fetuin-A in HFD mice significantly and regulated high-glucose- or palmitate-induced fetuin-A expression to increase insulin sensitivity through a GPR40/PLC/PKC pathway in HepG2 cells.	GW9508	31-38	alpha-2-HS-glycoprotein	Mus musculus	159-167
23341496-8	2013	Furthermore, administration of GW-9508 decreased the hepatic expression of fetuin-A in HFD mice significantly and regulated high-glucose- or palmitate-induced fetuin-A expression to increase insulin sensitivity through a GPR40/PLC/PKC pathway in HepG2 cells.	Glucose	129-136	alpha-2-HS-glycoprotein	Mus musculus	159-167
23341496-8	2013	Furthermore, administration of GW-9508 decreased the hepatic expression of fetuin-A in HFD mice significantly and regulated high-glucose- or palmitate-induced fetuin-A expression to increase insulin sensitivity through a GPR40/PLC/PKC pathway in HepG2 cells.	Palmitates	141-150	alpha-2-HS-glycoprotein	Mus musculus	159-167
23943623-4	2013	In adipocytes, fatty acid induces FetA gene and protein expressions, resulting in its copious release.	Fatty Acids	15-25	alpha-2-HS-glycoprotein	Mus musculus	34-38
15374947-6	2004	Furthermore, TGF-beta-mediated suppression of immune cell function was exaggerated in Ahsg-/- animals, as shown by inhibition of macrophage activation and reduction in 12-O-tetradecanoylphorbol 13-acetate-induced cutaneous inflammation.	Tetradecanoylphorbol Acetate	168-204	alpha-2-HS-glycoprotein	Mus musculus	86-90
22842477-6	2012	FFA-induced proinflammatory cytokine expression in adipocytes occurred only in the presence of both FetA and Tlr4; removing either of them prevented FFA-induced insulin resistance.	Fatty Acids, Nonesterified	0-3	alpha-2-HS-glycoprotein	Mus musculus	100-104
22842477-7	2012	We further found that FetA, through its terminal galactoside moiety, directly binds the residues of Leu100-Gly123 and Thr493-Thr516 in Tlr4.	Galactosides	49-60	alpha-2-HS-glycoprotein	Mus musculus	22-26
22842477-8	2012	FFAs did not produce insulin resistance in adipocytes with mutated Tlr4 or galactoside-cleaved FetA.	Galactosides	75-86	alpha-2-HS-glycoprotein	Mus musculus	95-99
17389622-0	2007	Fetuin-A (AHSG) prevents extraosseous calcification induced by uraemia and phosphate challenge in mice.	Phosphates	75-84	alpha-2-HS-glycoprotein	Mus musculus	0-8
17389622-0	2007	Fetuin-A (AHSG) prevents extraosseous calcification induced by uraemia and phosphate challenge in mice.	Phosphates	75-84	alpha-2-HS-glycoprotein	Mus musculus	10-14
17389622-8	2007	Fetuin-A-deficient mice with CKD and high phosphate diet had only a moderately elevated serum calcium phosphate product (6.9 +/- 1.4 mmol(2)/l(2)), but suffered severe calcification of kidney, heart and lung.	Phosphates	42-51	alpha-2-HS-glycoprotein	Mus musculus	0-8
17389622-8	2007	Fetuin-A-deficient mice with CKD and high phosphate diet had only a moderately elevated serum calcium phosphate product (6.9 +/- 1.4 mmol(2)/l(2)), but suffered severe calcification of kidney, heart and lung.	calcium phosphate	94-111	alpha-2-HS-glycoprotein	Mus musculus	0-8
16595698-0	2006	CCAAT enhancer binding protein beta and hepatocyte nuclear factor 3beta are necessary and sufficient to mediate dexamethasone-induced up-regulation of alpha2HS-glycoprotein/fetuin-A gene expression.	Dexamethasone	112-125	alpha-2-HS-glycoprotein	Mus musculus	151-172
16595698-0	2006	CCAAT enhancer binding protein beta and hepatocyte nuclear factor 3beta are necessary and sufficient to mediate dexamethasone-induced up-regulation of alpha2HS-glycoprotein/fetuin-A gene expression.	Dexamethasone	112-125	alpha-2-HS-glycoprotein	Mus musculus	173-181
16595698-4	2006	Using reporter gene assays in hepatoma cells combined with electrophoretic mobility shift assays we determined that dexamethasone up-regulates hepatic Ahsg.	Dexamethasone	116-129	alpha-2-HS-glycoprotein	Mus musculus	151-155
16595698-5	2006	A steroid response unit at position -146/-119 within the mouse Ahsg promoter mediates the glucocorticoid-induced increase of Ahsg mRNA.	Steroids	2-9	alpha-2-HS-glycoprotein	Mus musculus	63-67
16595698-5	2006	A steroid response unit at position -146/-119 within the mouse Ahsg promoter mediates the glucocorticoid-induced increase of Ahsg mRNA.	Steroids	2-9	alpha-2-HS-glycoprotein	Mus musculus	125-129
22619360-9	2012	Moreover, treatment with 4-phenylbutyrate in both streptozotocin-induced and high-fat diet-induced diabetic mice not only decreased hepatic fetuin-A levels but also improved hyperglycemia.	4-phenylbutyric acid	25-41	alpha-2-HS-glycoprotein	Mus musculus	140-148
22619360-9	2012	Moreover, treatment with 4-phenylbutyrate in both streptozotocin-induced and high-fat diet-induced diabetic mice not only decreased hepatic fetuin-A levels but also improved hyperglycemia.	Streptozocin	50-64	alpha-2-HS-glycoprotein	Mus musculus	140-148
15885488-1	2005	alpha2-HS-glycoprotein (Ahsg), also known as fetuin is a serum and bone resident glycoprotein, which binds to TGF-beta superfamily members including bone morphogenetic proteins (BMP) and inhibits dexamethasone-induced osteogenesis in bone marrow cultures in vitro.	Dexamethasone	196-209	alpha-2-HS-glycoprotein	Mus musculus	0-22
15885488-1	2005	alpha2-HS-glycoprotein (Ahsg), also known as fetuin is a serum and bone resident glycoprotein, which binds to TGF-beta superfamily members including bone morphogenetic proteins (BMP) and inhibits dexamethasone-induced osteogenesis in bone marrow cultures in vitro.	Dexamethasone	196-209	alpha-2-HS-glycoprotein	Mus musculus	24-28
12897203-3	2003	Ahsg-deficient mice are phenotypically normal, but develop severe calcification of various organs on a mineral and vitamin D-rich diet and on a normal diet when the deficiency is combined with a DBA/2 genetic background.	Vitamin D	115-124	alpha-2-HS-glycoprotein	Mus musculus	0-4
12556469-2	2003	Genetic evidence from mutant mice suggests that alpha(2)-HS glycoprotein/fetuin-A (Ahsg) is a systemic inhibitor of precipitation of basic calcium phosphate preventing unwanted calcification.	basic calcium phosphate	133-156	alpha-2-HS-glycoprotein	Mus musculus	48-72
12556469-2	2003	Genetic evidence from mutant mice suggests that alpha(2)-HS glycoprotein/fetuin-A (Ahsg) is a systemic inhibitor of precipitation of basic calcium phosphate preventing unwanted calcification.	basic calcium phosphate	133-156	alpha-2-HS-glycoprotein	Mus musculus	73-81
12556469-2	2003	Genetic evidence from mutant mice suggests that alpha(2)-HS glycoprotein/fetuin-A (Ahsg) is a systemic inhibitor of precipitation of basic calcium phosphate preventing unwanted calcification.	basic calcium phosphate	133-156	alpha-2-HS-glycoprotein	Mus musculus	83-87
12556469-3	2003	Using electron microscopy and dynamic light scattering, we demonstrate that precipitation inhibition by Ahsg is caused by the transient formation of soluble, colloidal spheres, containing Ahsg, calcium, and phosphate.	Calcium	194-201	alpha-2-HS-glycoprotein	Mus musculus	104-108
12556469-3	2003	Using electron microscopy and dynamic light scattering, we demonstrate that precipitation inhibition by Ahsg is caused by the transient formation of soluble, colloidal spheres, containing Ahsg, calcium, and phosphate.	Phosphates	207-216	alpha-2-HS-glycoprotein	Mus musculus	104-108
12556469-5	2003	Solubilization in Ahsg-containing calciprotein particles provides a novel conceptual framework to explain how insoluble calcium precipitates may be transported and removed in the bodies of mammals.	Calcium	120-127	alpha-2-HS-glycoprotein	Mus musculus	18-22
12556469-6	2003	Mutational analysis showed that the basic calcium phosphate precipitation inhibition activity resides in the amino-terminal cystatin-like domain D1 of Ahsg.	basic calcium phosphate	36-59	alpha-2-HS-glycoprotein	Mus musculus	151-155
12556469-7	2003	A structure-function analysis of wild type and mutant forms of cystatin-like domains from Ahsg, full-length fetuin-B, histidine-rich glycoprotein, and kininogen demonstrated that Ahsg domain D1 is most efficient in inhibiting basic calcium phosphate precipitation.	basic calcium phosphate	226-249	alpha-2-HS-glycoprotein	Mus musculus	179-183