Tetratricopeptide repeat/TPR repeat, putative

Quick info Localization Expansion Sequence features Structure Function Putative motif mimicry Homologs Download

Quick info

Protein:

Gene product:

TPR repeat, putative

Species:

Leishmania donovani

UniProt:

A0A3S5H6L1_LEIDO

TriTrypDb:

LdBPK_120560.1 , LdCL_120011300 , LDHU3_12.0880

Length:

1013

Localization

Secreted promastigote


Source	Evidence on protein	Close homologs
Cuervo et al.	no	yes: 0
Hassani et al.	no	yes: 0
Forrest at al. (metacyclic)	no	yes: 0
Forrest at al. (procyclic)	no	yes: 0
Silverman et al.	no	yes: 0
Pissara et al.	no	yes: 0

Secreted amastigote


Source	Evidence on protein	Close homologs
Pires et al.	no	yes: 0

Exosome


Source	Evidence on protein	Close homologs
Silverman et al.	no	yes: 0

Glycosome


Source	Evidence on protein	Close homologs
Jamdhade et al.	no	yes: 0

Predictions


Source	Evidence on protein	Close homologs
DeepLoc
SignalP6	no	yes: 0, no: 5
NetGPI	no	yes: 0, no: 5

Cellular components
Term	Name	Level	Count
GO:0000151	ubiquitin ligase complex	3	1
GO:0000152	nuclear ubiquitin ligase complex	3	1
GO:0005680	anaphase-promoting complex	4	1
GO:0005737	cytoplasm	2	1
GO:0031461	cullin-RING ubiquitin ligase complex	4	1
GO:0032991	protein-containing complex	1	1
GO:0110165	cellular anatomical entity	1	1
GO:0140513	nuclear protein-containing complex	2	1
GO:0140535	intracellular protein-containing complex	2	1
GO:1902494	catalytic complex	2	1
GO:1990234	transferase complex	3	1

Expansion

Sequence features

A0A3S5H6L1

Sequence

MSA

Disorder

Secondary

Topology

Domains

SignalP

GPI

Phosphorylations

ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: A0A3S5H6L1

Function

Biological processes
Term	Name	Level	Count
GO:0006508	proteolysis	4	1
GO:0006511	ubiquitin-dependent protein catabolic process	7	1
GO:0006807	nitrogen compound metabolic process	2	1
GO:0007088	regulation of mitotic nuclear division	6	1
GO:0007091	metaphase/anaphase transition of mitotic cell cycle	5	1
GO:0007346	regulation of mitotic cell cycle	5	1
GO:0008152	metabolic process	1	1
GO:0009056	catabolic process	2	1
GO:0009057	macromolecule catabolic process	4	1
GO:0009987	cellular process	1	1
GO:0010498	proteasomal protein catabolic process	5	1
GO:0010564	regulation of cell cycle process	5	1
GO:0010638	positive regulation of organelle organization	6	1
GO:0010965	regulation of mitotic sister chromatid separation	6	1
GO:0016567	protein ubiquitination	7	1
GO:0019538	protein metabolic process	3	1
GO:0019941	modification-dependent protein catabolic process	6	1
GO:0022402	cell cycle process	2	1
GO:0030071	regulation of mitotic metaphase/anaphase transition	7	1
GO:0030163	protein catabolic process	4	1
GO:0031145	anaphase-promoting complex-dependent catabolic process	7	1
GO:0032446	protein modification by small protein conjugation	6	1
GO:0033043	regulation of organelle organization	5	1
GO:0033044	regulation of chromosome organization	6	1
GO:0033045	regulation of sister chromatid segregation	5	1
GO:0036211	protein modification process	4	1
GO:0043161	proteasome-mediated ubiquitin-dependent protein catabolic process	6	1
GO:0043170	macromolecule metabolic process	3	1
GO:0043412	macromolecule modification	4	1
GO:0043632	modification-dependent macromolecule catabolic process	5	1
GO:0044237	cellular metabolic process	2	1
GO:0044238	primary metabolic process	2	1
GO:0044248	cellular catabolic process	3	1
GO:0044260	obsolete cellular macromolecule metabolic process	3	1
GO:0044265	obsolete cellular macromolecule catabolic process	4	1
GO:0044770	cell cycle phase transition	3	1
GO:0044772	mitotic cell cycle phase transition	4	1
GO:0044784	metaphase/anaphase transition of cell cycle	4	1
GO:0045787	positive regulation of cell cycle	5	1
GO:0045840	positive regulation of mitotic nuclear division	7	1
GO:0045842	positive regulation of mitotic metaphase/anaphase transition	8	1
GO:0045931	positive regulation of mitotic cell cycle	6	1
GO:0048518	positive regulation of biological process	3	1
GO:0048522	positive regulation of cellular process	4	1
GO:0050789	regulation of biological process	2	1
GO:0050794	regulation of cellular process	3	1
GO:0051128	regulation of cellular component organization	4	1
GO:0051130	positive regulation of cellular component organization	5	1
GO:0051301	cell division	2	1
GO:0051603	proteolysis involved in protein catabolic process	5	1
GO:0051726	regulation of cell cycle	4	1
GO:0051783	regulation of nuclear division	6	1
GO:0051785	positive regulation of nuclear division	7	1
GO:0051983	regulation of chromosome segregation	4	1
GO:0065007	biological regulation	1	1
GO:0070647	protein modification by small protein conjugation or removal	5	1
GO:0071704	organic substance metabolic process	2	1
GO:0090068	positive regulation of cell cycle process	6	1
GO:1901564	organonitrogen compound metabolic process	3	1
GO:1901565	organonitrogen compound catabolic process	4	1
GO:1901575	organic substance catabolic process	3	1
GO:1901970	positive regulation of mitotic sister chromatid separation	7	1
GO:1901987	regulation of cell cycle phase transition	6	1
GO:1901989	positive regulation of cell cycle phase transition	7	1
GO:1901990	regulation of mitotic cell cycle phase transition	6	1
GO:1901992	positive regulation of mitotic cell cycle phase transition	7	1
GO:1902099	regulation of metaphase/anaphase transition of cell cycle	6	1
GO:1902101	positive regulation of metaphase/anaphase transition of cell cycle	7	1
GO:1903047	mitotic cell cycle process	3	1
GO:1905818	regulation of chromosome separation	5	1
GO:1905820	positive regulation of chromosome separation	6	1

Could not find GO molecular_function term for this entry.

Putative motif mimicry


Leishmania	From	To	Domain/Motif	Score
CLV_C14_Caspase3-7	136	140	PF00656	0.655
CLV_NRD_NRD_1	10	12	PF00675	0.638
CLV_NRD_NRD_1	740	742	PF00675	0.487
CLV_NRD_NRD_1	904	906	PF00675	0.840
CLV_PCSK_KEX2_1	10	12	PF00082	0.638
CLV_PCSK_KEX2_1	270	272	PF00082	0.711
CLV_PCSK_KEX2_1	575	577	PF00082	0.496
CLV_PCSK_KEX2_1	740	742	PF00082	0.487
CLV_PCSK_KEX2_1	903	905	PF00082	0.844
CLV_PCSK_PC1ET2_1	270	272	PF00082	0.711
CLV_PCSK_PC1ET2_1	575	577	PF00082	0.496
CLV_PCSK_SKI1_1	438	442	PF00082	0.529
CLV_PCSK_SKI1_1	478	482	PF00082	0.600
CLV_PCSK_SKI1_1	614	618	PF00082	0.576
CLV_PCSK_SKI1_1	741	745	PF00082	0.475
CLV_PCSK_SKI1_1	828	832	PF00082	0.621
CLV_PCSK_SKI1_1	86	90	PF00082	0.526
CLV_Separin_Metazoa	107	111	PF03568	0.586
CLV_Separin_Metazoa	150	154	PF03568	0.647
DEG_APCC_DBOX_1	577	585	PF00400	0.474
DEG_Nend_UBRbox_2	1	3	PF02207	0.537
DEG_SCF_FBW7_1	441	448	PF00400	0.522
DEG_SPOP_SBC_1	113	117	PF00917	0.533
DEG_SPOP_SBC_1	272	276	PF00917	0.698
DEG_SPOP_SBC_1	288	292	PF00917	0.515
DEG_SPOP_SBC_1	479	483	PF00917	0.710
DEG_SPOP_SBC_1	796	800	PF00917	0.529
DEG_SPOP_SBC_1	971	975	PF00917	0.564
DEG_SPOP_SBC_1	990	994	PF00917	0.627
DOC_ANK_TNKS_1	788	795	PF00023	0.517
DOC_CDC14_PxL_1	25	33	PF14671	0.620
DOC_CKS1_1	524	529	PF01111	0.482
DOC_CYCLIN_yCln2_LP_2	32	38	PF00134	0.655
DOC_CYCLIN_yCln2_LP_2	775	781	PF00134	0.504
DOC_MAPK_DCC_7	156	166	PF00069	0.546
DOC_MAPK_gen_1	575	581	PF00069	0.489
DOC_PP2B_LxvP_1	144	147	PF13499	0.701
DOC_PP2B_LxvP_1	228	231	PF13499	0.728
DOC_PP2B_LxvP_1	32	35	PF13499	0.559
DOC_PP2B_LxvP_1	775	778	PF13499	0.507
DOC_PP2B_LxvP_1	856	859	PF13499	0.693
DOC_USP7_MATH_1	1003	1007	PF00917	0.776
DOC_USP7_MATH_1	113	117	PF00917	0.642
DOC_USP7_MATH_1	121	125	PF00917	0.601
DOC_USP7_MATH_1	192	196	PF00917	0.744
DOC_USP7_MATH_1	259	263	PF00917	0.573
DOC_USP7_MATH_1	27	31	PF00917	0.626
DOC_USP7_MATH_1	302	306	PF00917	0.787
DOC_USP7_MATH_1	389	393	PF00917	0.571
DOC_USP7_MATH_1	445	449	PF00917	0.516
DOC_USP7_MATH_1	456	460	PF00917	0.471
DOC_USP7_MATH_1	510	514	PF00917	0.505
DOC_USP7_MATH_1	52	56	PF00917	0.622
DOC_USP7_MATH_1	748	752	PF00917	0.471
DOC_USP7_MATH_1	75	79	PF00917	0.589
DOC_USP7_MATH_1	766	770	PF00917	0.394
DOC_USP7_MATH_1	788	792	PF00917	0.620
DOC_USP7_MATH_1	874	878	PF00917	0.690
DOC_USP7_MATH_1	880	884	PF00917	0.633
DOC_USP7_MATH_1	888	892	PF00917	0.575
DOC_USP7_MATH_1	915	919	PF00917	0.817
DOC_USP7_MATH_1	921	925	PF00917	0.689
DOC_USP7_MATH_1	971	975	PF00917	0.659
DOC_USP7_MATH_1	978	982	PF00917	0.673
DOC_USP7_MATH_1	990	994	PF00917	0.604
DOC_WW_Pin1_4	324	329	PF00397	0.645
DOC_WW_Pin1_4	331	336	PF00397	0.602
DOC_WW_Pin1_4	441	446	PF00397	0.530
DOC_WW_Pin1_4	465	470	PF00397	0.702
DOC_WW_Pin1_4	48	53	PF00397	0.569
DOC_WW_Pin1_4	489	494	PF00397	0.737
DOC_WW_Pin1_4	501	506	PF00397	0.606
DOC_WW_Pin1_4	523	528	PF00397	0.490
DOC_WW_Pin1_4	729	734	PF00397	0.552
DOC_WW_Pin1_4	762	767	PF00397	0.516
DOC_WW_Pin1_4	804	809	PF00397	0.698
DOC_WW_Pin1_4	815	820	PF00397	0.544
DOC_WW_Pin1_4	870	875	PF00397	0.672
LIG_14-3-3_CanoR_1	153	163	PF00244	0.614
LIG_14-3-3_CanoR_1	271	281	PF00244	0.699
LIG_14-3-3_CanoR_1	489	493	PF00244	0.621
LIG_14-3-3_CanoR_1	578	588	PF00244	0.474
LIG_14-3-3_CanoR_1	621	627	PF00244	0.477
LIG_14-3-3_CanoR_1	787	793	PF00244	0.558
LIG_14-3-3_CanoR_1	797	806	PF00244	0.715
LIG_Actin_WH2_2	384	400	PF00022	0.493
LIG_Actin_WH2_2	436	454	PF00022	0.523
LIG_APCC_ABBAyCdc20_2	754	760	PF00400	0.485
LIG_BIR_III_2	352	356	PF00653	0.585
LIG_BRCT_BRCA1_1	326	330	PF00533	0.710
LIG_BRCT_BRCA1_1	382	386	PF00533	0.513
LIG_BRCT_BRCA1_1	461	465	PF00533	0.623
LIG_BRCT_BRCA1_1	519	523	PF00533	0.482
LIG_BRCT_BRCA1_1	60	64	PF00533	0.671
LIG_Clathr_ClatBox_1	359	363	PF01394	0.604
LIG_EVH1_2	942	946	PF00568	0.648
LIG_FHA_1	155	161	PF00498	0.616
LIG_FHA_1	289	295	PF00498	0.717
LIG_FHA_1	31	37	PF00498	0.541
LIG_FHA_1	354	360	PF00498	0.707
LIG_FHA_1	383	389	PF00498	0.476
LIG_FHA_1	502	508	PF00498	0.684
LIG_FHA_1	645	651	PF00498	0.422
LIG_FHA_1	688	694	PF00498	0.592
LIG_FHA_1	742	748	PF00498	0.476
LIG_FHA_1	768	774	PF00498	0.475
LIG_FHA_2	572	578	PF00498	0.506
LIG_FHA_2	621	627	PF00498	0.477
LIG_FHA_2	653	659	PF00498	0.459
LIG_FHA_2	850	856	PF00498	0.644
LIG_LIR_Gen_1	168	177	PF02991	0.561
LIG_LIR_Gen_1	327	336	PF02991	0.654
LIG_LIR_Gen_1	513	524	PF02991	0.483
LIG_LIR_Gen_1	548	559	PF02991	0.495
LIG_LIR_Gen_1	567	573	PF02991	0.442
LIG_LIR_Gen_1	631	641	PF02991	0.405
LIG_LIR_Gen_1	78	89	PF02991	0.537
LIG_LIR_Nem_3	168	173	PF02991	0.552
LIG_LIR_Nem_3	327	333	PF02991	0.768
LIG_LIR_Nem_3	425	430	PF02991	0.453
LIG_LIR_Nem_3	513	519	PF02991	0.475
LIG_LIR_Nem_3	548	554	PF02991	0.489
LIG_LIR_Nem_3	558	564	PF02991	0.607
LIG_LIR_Nem_3	567	571	PF02991	0.436
LIG_LIR_Nem_3	631	636	PF02991	0.405
LIG_LIR_Nem_3	732	738	PF02991	0.606
LIG_LIR_Nem_3	78	84	PF02991	0.552
LIG_PCNA_TLS_4	86	94	PF02747	0.503
LIG_PCNA_yPIPBox_3	1001	1009	PF02747	0.624
LIG_PCNA_yPIPBox_3	595	606	PF02747	0.441
LIG_Pex14_2	519	523	PF04695	0.482
LIG_PTB_Apo_2	567	574	PF02174	0.449
LIG_PTB_Apo_2	746	753	PF02174	0.504
LIG_PTB_Phospho_1	567	573	PF10480	0.442
LIG_PTB_Phospho_1	746	752	PF10480	0.501
LIG_Rb_LxCxE_1	716	734	PF01857	0.507
LIG_Rb_pABgroove_1	560	568	PF01858	0.472
LIG_SH2_CRK	551	555	PF00017	0.485
LIG_SH2_CRK	568	572	PF00017	0.433
LIG_SH2_GRB2like	568	571	PF00017	0.434
LIG_SH2_PTP2	606	609	PF00017	0.455
LIG_SH2_PTP2	640	643	PF00017	0.405
LIG_SH2_SRC	566	569	PF00017	0.447
LIG_SH2_SRC	640	643	PF00017	0.405
LIG_SH2_STAP1	170	174	PF00017	0.548
LIG_SH2_STAP1	568	572	PF00017	0.433
LIG_SH2_STAT3	537	540	PF00017	0.489
LIG_SH2_STAT5	216	219	PF00017	0.646
LIG_SH2_STAT5	365	368	PF00017	0.518
LIG_SH2_STAT5	561	564	PF00017	0.516
LIG_SH2_STAT5	573	576	PF00017	0.564
LIG_SH2_STAT5	606	609	PF00017	0.455
LIG_SH2_STAT5	640	643	PF00017	0.517
LIG_SH2_STAT5	738	741	PF00017	0.485
LIG_SH2_STAT5	752	755	PF00017	0.366
LIG_SH2_STAT5	758	761	PF00017	0.278
LIG_SH2_STAT5	784	787	PF00017	0.502
LIG_SH2_STAT5	91	94	PF00017	0.533
LIG_SH3_2	493	498	PF14604	0.630
LIG_SH3_3	117	123	PF00018	0.626
LIG_SH3_3	490	496	PF00018	0.687
LIG_SH3_3	502	508	PF00018	0.582
LIG_SH3_3	521	527	PF00018	0.345
LIG_SH3_3	692	698	PF00018	0.487
LIG_SH3_3	730	736	PF00018	0.532
LIG_SH3_CIN85_PxpxPR_1	493	498	PF14604	0.630
LIG_Sin3_3	632	639	PF02671	0.405
LIG_TYR_ITAM	548	564	PF00017	0.492
LIG_WW_3	495	499	PF00397	0.693
MOD_CDK_SPxxK_3	335	342	PF00069	0.708
MOD_CK1_1	21	27	PF00069	0.608
MOD_CK1_1	233	239	PF00069	0.705
MOD_CK1_1	287	293	PF00069	0.631
MOD_CK1_1	30	36	PF00069	0.462
MOD_CK1_1	307	313	PF00069	0.517
MOD_CK1_1	331	337	PF00069	0.724
MOD_CK1_1	459	465	PF00069	0.627
MOD_CK1_1	48	54	PF00069	0.585
MOD_CK1_1	729	735	PF00069	0.542
MOD_CK1_1	750	756	PF00069	0.499
MOD_CK1_1	800	806	PF00069	0.713
MOD_CK1_1	814	820	PF00069	0.654
MOD_CK1_1	920	926	PF00069	0.692
MOD_CK1_1	985	991	PF00069	0.741
MOD_CK1_1	992	998	PF00069	0.766
MOD_CK2_1	130	136	PF00069	0.590
MOD_CK2_1	233	239	PF00069	0.705
MOD_CK2_1	652	658	PF00069	0.405
MOD_CK2_1	787	793	PF00069	0.672
MOD_CK2_1	849	855	PF00069	0.638
MOD_GlcNHglycan	193	197	PF01048	0.708
MOD_GlcNHglycan	199	202	PF01048	0.651
MOD_GlcNHglycan	232	235	PF01048	0.617
MOD_GlcNHglycan	261	264	PF01048	0.672
MOD_GlcNHglycan	267	270	PF01048	0.694
MOD_GlcNHglycan	276	279	PF01048	0.630
MOD_GlcNHglycan	286	289	PF01048	0.612
MOD_GlcNHglycan	302	305	PF01048	0.585
MOD_GlcNHglycan	306	309	PF01048	0.545
MOD_GlcNHglycan	382	385	PF01048	0.559
MOD_GlcNHglycan	447	450	PF01048	0.532
MOD_GlcNHglycan	458	461	PF01048	0.553
MOD_GlcNHglycan	471	474	PF01048	0.716
MOD_GlcNHglycan	60	63	PF01048	0.667
MOD_GlcNHglycan	77	80	PF01048	0.581
MOD_GlcNHglycan	820	823	PF01048	0.624
MOD_GlcNHglycan	859	862	PF01048	0.719
MOD_GlcNHglycan	876	879	PF01048	0.624
MOD_GlcNHglycan	889	893	PF01048	0.655
MOD_GlcNHglycan	910	913	PF01048	0.872
MOD_GlcNHglycan	919	922	PF01048	0.793
MOD_GlcNHglycan	923	926	PF01048	0.729
MOD_GlcNHglycan	936	939	PF01048	0.548
MOD_GlcNHglycan	980	983	PF01048	0.812
MOD_GlcNHglycan	984	987	PF01048	0.755
MOD_GSK3_1	109	116	PF00069	0.713
MOD_GSK3_1	122	129	PF00069	0.611
MOD_GSK3_1	180	187	PF00069	0.671
MOD_GSK3_1	229	236	PF00069	0.744
MOD_GSK3_1	259	266	PF00069	0.578
MOD_GSK3_1	280	287	PF00069	0.648
MOD_GSK3_1	296	303	PF00069	0.572
MOD_GSK3_1	324	331	PF00069	0.700
MOD_GSK3_1	441	448	PF00069	0.522
MOD_GSK3_1	465	472	PF00069	0.811
MOD_GSK3_1	48	55	PF00069	0.611
MOD_GSK3_1	485	492	PF00069	0.668
MOD_GSK3_1	580	587	PF00069	0.539
MOD_GSK3_1	723	730	PF00069	0.520
MOD_GSK3_1	762	769	PF00069	0.514
MOD_GSK3_1	796	803	PF00069	0.658
MOD_GSK3_1	811	818	PF00069	0.548
MOD_GSK3_1	870	877	PF00069	0.705
MOD_GSK3_1	915	922	PF00069	0.792
MOD_GSK3_1	930	937	PF00069	0.600
MOD_GSK3_1	978	985	PF00069	0.837
MOD_GSK3_1	988	995	PF00069	0.717
MOD_N-GLC_1	184	189	PF02516	0.671
MOD_N-GLC_1	331	336	PF02516	0.698
MOD_N-GLC_1	644	649	PF02516	0.405
MOD_N-GLC_1	748	753	PF02516	0.518
MOD_N-GLC_1	811	816	PF02516	0.639
MOD_N-GLC_1	915	920	PF02516	0.795
MOD_NEK2_1	109	114	PF00069	0.620
MOD_NEK2_1	155	160	PF00069	0.593
MOD_NEK2_1	197	202	PF00069	0.680
MOD_NEK2_1	528	533	PF00069	0.454
MOD_NEK2_1	579	584	PF00069	0.537
MOD_NEK2_1	795	800	PF00069	0.534
MOD_NEK2_1	946	951	PF00069	0.675
MOD_PIKK_1	1003	1009	PF00454	0.549
MOD_PIKK_1	123	129	PF00454	0.653
MOD_PIKK_1	184	190	PF00454	0.712
MOD_PIKK_1	528	534	PF00454	0.452
MOD_PIKK_1	985	991	PF00454	0.712
MOD_PIKK_1	992	998	PF00454	0.646
MOD_PKA_1	903	909	PF00069	0.763
MOD_PKA_2	109	115	PF00069	0.636
MOD_PKA_2	155	161	PF00069	0.609
MOD_PKA_2	488	494	PF00069	0.612
MOD_PKA_2	620	626	PF00069	0.478
MOD_PKA_2	788	794	PF00069	0.561
MOD_PKA_2	796	802	PF00069	0.570
MOD_PKA_2	903	909	PF00069	0.811
MOD_PKB_1	378	386	PF00069	0.527
MOD_Plk_1	21	27	PF00069	0.676
MOD_Plk_1	748	754	PF00069	0.519
MOD_Plk_1	811	817	PF00069	0.650
MOD_Plk_1	915	921	PF00069	0.788
MOD_Plk_4	15	21	PF00069	0.631
MOD_Plk_4	165	171	PF00069	0.537
MOD_Plk_4	27	33	PF00069	0.688
MOD_Plk_4	316	322	PF00069	0.694
MOD_Plk_4	364	370	PF00069	0.525
MOD_Plk_4	382	388	PF00069	0.372
MOD_Plk_4	52	58	PF00069	0.615
MOD_Plk_4	584	590	PF00069	0.483
MOD_Plk_4	800	806	PF00069	0.715
MOD_Plk_4	811	817	PF00069	0.588
MOD_ProDKin_1	324	330	PF00069	0.648
MOD_ProDKin_1	331	337	PF00069	0.604
MOD_ProDKin_1	441	447	PF00069	0.523
MOD_ProDKin_1	465	471	PF00069	0.704
MOD_ProDKin_1	48	54	PF00069	0.568
MOD_ProDKin_1	489	495	PF00069	0.736
MOD_ProDKin_1	501	507	PF00069	0.603
MOD_ProDKin_1	523	529	PF00069	0.484
MOD_ProDKin_1	729	735	PF00069	0.542
MOD_ProDKin_1	762	768	PF00069	0.513
MOD_ProDKin_1	804	810	PF00069	0.699
MOD_ProDKin_1	815	821	PF00069	0.540
MOD_ProDKin_1	870	876	PF00069	0.672
MOD_SUMO_for_1	93	96	PF00179	0.519
TRG_DiLeu_BaEn_1	436	441	PF01217	0.499
TRG_DiLeu_BaEn_1	517	522	PF01217	0.472
TRG_DiLeu_BaEn_1	631	636	PF01217	0.405
TRG_DiLeu_BaEn_1	9	14	PF01217	0.508
TRG_DiLeu_BaEn_2	381	387	PF01217	0.513
TRG_DiLeu_BaLyEn_6	159	164	PF01217	0.505
TRG_DiLeu_BaLyEn_6	392	397	PF01217	0.497
TRG_ENDOCYTIC_2	170	173	PF00928	0.549
TRG_ENDOCYTIC_2	551	554	PF00928	0.575
TRG_ENDOCYTIC_2	561	564	PF00928	0.409
TRG_ENDOCYTIC_2	568	571	PF00928	0.434
TRG_ENDOCYTIC_2	605	608	PF00928	0.449
TRG_ENDOCYTIC_2	640	643	PF00928	0.405
TRG_ENDOCYTIC_2	674	677	PF00928	0.514
TRG_ER_diArg_1	377	380	PF00400	0.636
TRG_ER_diArg_1	450	453	PF00400	0.542
TRG_ER_diArg_1	541	544	PF00400	0.533
TRG_ER_diArg_1	739	741	PF00400	0.490
TRG_ER_diArg_1	903	905	PF00400	0.798
TRG_ER_diArg_1	947	950	PF00400	0.651
TRG_NES_CRM1_1	422	436	PF08389	0.446

Homologs


Protein	Taxonomy	Sequence identity	Coverage
A4H6X4	Leishmania braziliensis	80%	100%
E9AGE8	Leishmania infantum	100%	100%
E9ANY8	Leishmania mexicana (strain MHOM/GT/2001/U1103)	90%	100%
Q4QGN2	Leishmania major	91%	100%