TPR_REGION domain-containing protein

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

Quick info

Protein:

Gene product:

TPR repeat, putative

Species:

Leishmania mexicana

UniProt:

E9ANY8_LEIMU

TriTrypDb:

LmxM.12.0610

Length:

1066

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

E9ANY8

Sequence

MSA

Disorder

Secondary

Topology

Domains

SignalP

GPI

Phosphorylations

ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: E9ANY8

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	196	200	PF00656	0.646
CLV_C14_Caspase3-7	63	67	PF00656	0.506
CLV_NRD_NRD_1	74	76	PF00675	0.634
CLV_NRD_NRD_1	795	797	PF00675	0.540
CLV_NRD_NRD_1	959	961	PF00675	0.747
CLV_PCSK_KEX2_1	330	332	PF00082	0.709
CLV_PCSK_KEX2_1	630	632	PF00082	0.476
CLV_PCSK_KEX2_1	74	76	PF00082	0.634
CLV_PCSK_KEX2_1	795	797	PF00082	0.540
CLV_PCSK_KEX2_1	958	960	PF00082	0.742
CLV_PCSK_PC1ET2_1	330	332	PF00082	0.709
CLV_PCSK_PC1ET2_1	630	632	PF00082	0.476
CLV_PCSK_SKI1_1	146	150	PF00082	0.514
CLV_PCSK_SKI1_1	498	502	PF00082	0.511
CLV_PCSK_SKI1_1	669	673	PF00082	0.436
CLV_PCSK_SKI1_1	796	800	PF00082	0.455
CLV_PCSK_SKI1_1	883	887	PF00082	0.558
CLV_Separin_Metazoa	167	171	PF03568	0.548
CLV_Separin_Metazoa	210	214	PF03568	0.645
DEG_APCC_DBOX_1	632	640	PF00400	0.455
DEG_Nend_UBRbox_2	1	3	PF02207	0.569
DEG_SCF_FBW7_1	501	508	PF00400	0.504
DEG_SPOP_SBC_1	1045	1049	PF00917	0.621
DEG_SPOP_SBC_1	252	256	PF00917	0.609
DEG_SPOP_SBC_1	332	336	PF00917	0.689
DEG_SPOP_SBC_1	348	352	PF00917	0.631
DOC_ANK_TNKS_1	843	850	PF00023	0.470
DOC_CDC14_PxL_1	89	97	PF14671	0.606
DOC_CKS1_1	579	584	PF01111	0.494
DOC_CKS1_1	96	101	PF01111	0.499
DOC_CYCLIN_yCln2_LP_2	830	836	PF00134	0.457
DOC_CYCLIN_yCln2_LP_2	96	102	PF00134	0.613
DOC_MAPK_DCC_7	216	226	PF00069	0.629
DOC_MAPK_gen_1	140	149	PF00069	0.449
DOC_MAPK_gen_1	630	636	PF00069	0.469
DOC_PP2B_LxvP_1	204	207	PF13499	0.691
DOC_PP2B_LxvP_1	288	291	PF13499	0.727
DOC_PP2B_LxvP_1	830	833	PF13499	0.467
DOC_PP2B_LxvP_1	911	914	PF13499	0.598
DOC_USP7_MATH_1	1035	1039	PF00917	0.632
DOC_USP7_MATH_1	1043	1047	PF00917	0.584
DOC_USP7_MATH_1	1058	1062	PF00917	0.653
DOC_USP7_MATH_1	135	139	PF00917	0.514
DOC_USP7_MATH_1	252	256	PF00917	0.712
DOC_USP7_MATH_1	291	295	PF00917	0.614
DOC_USP7_MATH_1	362	366	PF00917	0.707
DOC_USP7_MATH_1	379	383	PF00917	0.612
DOC_USP7_MATH_1	385	389	PF00917	0.750
DOC_USP7_MATH_1	449	453	PF00917	0.576
DOC_USP7_MATH_1	505	509	PF00917	0.501
DOC_USP7_MATH_1	519	523	PF00917	0.478
DOC_USP7_MATH_1	565	569	PF00917	0.487
DOC_USP7_MATH_1	803	807	PF00917	0.452
DOC_USP7_MATH_1	821	825	PF00917	0.428
DOC_USP7_MATH_1	843	847	PF00917	0.496
DOC_USP7_MATH_1	91	95	PF00917	0.596
DOC_USP7_MATH_1	926	930	PF00917	0.653
DOC_USP7_MATH_1	935	939	PF00917	0.627
DOC_USP7_MATH_1	943	947	PF00917	0.581
DOC_USP7_MATH_1	972	976	PF00917	0.660
DOC_USP7_MATH_2	50	56	PF00917	0.571
DOC_WW_Pin1_4	108	113	PF00397	0.555
DOC_WW_Pin1_4	133	138	PF00397	0.622
DOC_WW_Pin1_4	2	7	PF00397	0.553
DOC_WW_Pin1_4	33	38	PF00397	0.560
DOC_WW_Pin1_4	391	396	PF00397	0.701
DOC_WW_Pin1_4	44	49	PF00397	0.560
DOC_WW_Pin1_4	501	506	PF00397	0.511
DOC_WW_Pin1_4	525	530	PF00397	0.671
DOC_WW_Pin1_4	544	549	PF00397	0.807
DOC_WW_Pin1_4	556	561	PF00397	0.588
DOC_WW_Pin1_4	578	583	PF00397	0.503
DOC_WW_Pin1_4	784	789	PF00397	0.670
DOC_WW_Pin1_4	817	822	PF00397	0.518
DOC_WW_Pin1_4	859	864	PF00397	0.636
DOC_WW_Pin1_4	870	875	PF00397	0.520
DOC_WW_Pin1_4	95	100	PF00397	0.498
LIG_14-3-3_CanoR_1	181	191	PF00244	0.527
LIG_14-3-3_CanoR_1	213	223	PF00244	0.600
LIG_14-3-3_CanoR_1	331	341	PF00244	0.688
LIG_14-3-3_CanoR_1	54	61	PF00244	0.514
LIG_14-3-3_CanoR_1	608	613	PF00244	0.398
LIG_14-3-3_CanoR_1	633	643	PF00244	0.456
LIG_14-3-3_CanoR_1	676	682	PF00244	0.574
LIG_14-3-3_CanoR_1	842	848	PF00244	0.502
LIG_14-3-3_CanoR_1	852	857	PF00244	0.532
LIG_Actin_WH2_2	444	460	PF00022	0.489
LIG_Actin_WH2_2	496	514	PF00022	0.505
LIG_APCC_ABBAyCdc20_2	809	815	PF00400	0.459
LIG_BIR_III_2	412	416	PF00653	0.578
LIG_BRCT_BRCA1_1	120	124	PF00533	0.656
LIG_BRCT_BRCA1_1	386	390	PF00533	0.682
LIG_BRCT_BRCA1_1	442	446	PF00533	0.541
LIG_BRCT_BRCA1_1	521	525	PF00533	0.597
LIG_BRCT_BRCA1_1	574	578	PF00533	0.466
LIG_Clathr_ClatBox_1	419	423	PF01394	0.582
LIG_EVH1_2	997	1001	PF00568	0.574
LIG_FHA_1	1028	1034	PF00498	0.569
LIG_FHA_1	187	193	PF00498	0.536
LIG_FHA_1	215	221	PF00498	0.599
LIG_FHA_1	352	358	PF00498	0.632
LIG_FHA_1	414	420	PF00498	0.651
LIG_FHA_1	44	50	PF00498	0.588
LIG_FHA_1	557	563	PF00498	0.755
LIG_FHA_1	700	706	PF00498	0.385
LIG_FHA_1	743	749	PF00498	0.482
LIG_FHA_1	797	803	PF00498	0.458
LIG_FHA_1	823	829	PF00498	0.456
LIG_FHA_1	95	101	PF00498	0.508
LIG_FHA_2	151	157	PF00498	0.463
LIG_FHA_2	348	354	PF00498	0.644
LIG_FHA_2	58	64	PF00498	0.495
LIG_FHA_2	627	633	PF00498	0.468
LIG_FHA_2	676	682	PF00498	0.460
LIG_FHA_2	708	714	PF00498	0.385
LIG_FHA_2	905	911	PF00498	0.542
LIG_LIR_Apic_2	189	193	PF02991	0.594
LIG_LIR_Apic_2	2	6	PF02991	0.528
LIG_LIR_Gen_1	111	119	PF02991	0.498
LIG_LIR_Gen_1	138	149	PF02991	0.507
LIG_LIR_Gen_1	228	237	PF02991	0.531
LIG_LIR_Gen_1	387	396	PF02991	0.637
LIG_LIR_Gen_1	568	579	PF02991	0.465
LIG_LIR_Gen_1	603	614	PF02991	0.474
LIG_LIR_Gen_1	622	628	PF02991	0.246
LIG_LIR_Gen_1	686	696	PF02991	0.527
LIG_LIR_Gen_1	853	863	PF02991	0.533
LIG_LIR_Nem_3	111	117	PF02991	0.548
LIG_LIR_Nem_3	138	144	PF02991	0.516
LIG_LIR_Nem_3	228	233	PF02991	0.572
LIG_LIR_Nem_3	387	393	PF02991	0.749
LIG_LIR_Nem_3	478	484	PF02991	0.415
LIG_LIR_Nem_3	485	490	PF02991	0.443
LIG_LIR_Nem_3	568	574	PF02991	0.582
LIG_LIR_Nem_3	603	609	PF02991	0.470
LIG_LIR_Nem_3	613	619	PF02991	0.381
LIG_LIR_Nem_3	622	626	PF02991	0.241
LIG_LIR_Nem_3	686	691	PF02991	0.527
LIG_LIR_Nem_3	787	793	PF02991	0.490
LIG_LIR_Nem_3	853	859	PF02991	0.524
LIG_PCNA_yPIPBox_3	1056	1064	PF02747	0.605
LIG_PCNA_yPIPBox_3	650	661	PF02747	0.421
LIG_Pex14_2	574	578	PF04695	0.466
LIG_PTB_Apo_2	622	629	PF02174	0.432
LIG_PTB_Apo_2	801	808	PF02174	0.481
LIG_PTB_Phospho_1	622	628	PF10480	0.425
LIG_PTB_Phospho_1	801	807	PF10480	0.477
LIG_Rb_LxCxE_1	771	789	PF01857	0.485
LIG_Rb_pABgroove_1	615	623	PF01858	0.454
LIG_SH2_CRK	114	118	PF00017	0.498
LIG_SH2_CRK	606	610	PF00017	0.464
LIG_SH2_CRK	623	627	PF00017	0.257
LIG_SH2_CRK	856	860	PF00017	0.535
LIG_SH2_GRB2like	623	626	PF00017	0.416
LIG_SH2_NCK_1	114	118	PF00017	0.498
LIG_SH2_PTP2	661	664	PF00017	0.436
LIG_SH2_PTP2	695	698	PF00017	0.385
LIG_SH2_SRC	621	624	PF00017	0.443
LIG_SH2_SRC	695	698	PF00017	0.404
LIG_SH2_STAP1	230	234	PF00017	0.526
LIG_SH2_STAP1	623	627	PF00017	0.415
LIG_SH2_STAP1	856	860	PF00017	0.535
LIG_SH2_STAT3	592	595	PF00017	0.467
LIG_SH2_STAT5	151	154	PF00017	0.535
LIG_SH2_STAT5	276	279	PF00017	0.602
LIG_SH2_STAT5	425	428	PF00017	0.495
LIG_SH2_STAT5	616	619	PF00017	0.528
LIG_SH2_STAT5	628	631	PF00017	0.473
LIG_SH2_STAT5	661	664	PF00017	0.458
LIG_SH2_STAT5	695	698	PF00017	0.385
LIG_SH2_STAT5	793	796	PF00017	0.463
LIG_SH2_STAT5	807	810	PF00017	0.350
LIG_SH2_STAT5	813	816	PF00017	0.272
LIG_SH3_1	545	551	PF00018	0.611
LIG_SH3_2	548	553	PF14604	0.617
LIG_SH3_3	401	407	PF00018	0.558
LIG_SH3_3	524	530	PF00018	0.601
LIG_SH3_3	545	551	PF00018	0.816
LIG_SH3_3	557	563	PF00018	0.606
LIG_SH3_3	576	582	PF00018	0.344
LIG_SH3_3	747	753	PF00018	0.467
LIG_SH3_3	785	791	PF00018	0.509
LIG_SH3_3	958	964	PF00018	0.581
LIG_SH3_CIN85_PxpxPR_1	548	553	PF14604	0.617
LIG_Sin3_3	687	694	PF02671	0.385
LIG_TYR_ITAM	603	619	PF00017	0.472
LIG_WW_3	550	554	PF00397	0.678
MOD_CDK_SPxxK_3	133	140	PF00069	0.476
MOD_CDK_SPxxK_3	395	402	PF00069	0.684
MOD_CK1_1	1046	1052	PF00069	0.637
MOD_CK1_1	16	22	PF00069	0.521
MOD_CK1_1	23	29	PF00069	0.492
MOD_CK1_1	293	299	PF00069	0.695
MOD_CK1_1	347	353	PF00069	0.742
MOD_CK1_1	36	42	PF00069	0.530
MOD_CK1_1	381	387	PF00069	0.723
MOD_CK1_1	388	394	PF00069	0.774
MOD_CK1_1	4	10	PF00069	0.575
MOD_CK1_1	55	61	PF00069	0.490
MOD_CK1_1	784	790	PF00069	0.525
MOD_CK1_1	805	811	PF00069	0.504
MOD_CK1_1	85	91	PF00069	0.612
MOD_CK1_1	851	857	PF00069	0.569
MOD_CK1_1	869	875	PF00069	0.529
MOD_CK1_1	94	100	PF00069	0.516
MOD_CK1_1	970	976	PF00069	0.593
MOD_CK2_1	150	156	PF00069	0.470
MOD_CK2_1	293	299	PF00069	0.695
MOD_CK2_1	57	63	PF00069	0.535
MOD_CK2_1	707	713	PF00069	0.459
MOD_CK2_1	842	848	PF00069	0.502
MOD_CK2_1	904	910	PF00069	0.534
MOD_GlcNHglycan	1035	1038	PF01048	0.673
MOD_GlcNHglycan	1039	1042	PF01048	0.640
MOD_GlcNHglycan	120	123	PF01048	0.709
MOD_GlcNHglycan	137	140	PF01048	0.590
MOD_GlcNHglycan	15	18	PF01048	0.548
MOD_GlcNHglycan	22	25	PF01048	0.513
MOD_GlcNHglycan	259	262	PF01048	0.608
MOD_GlcNHglycan	327	330	PF01048	0.787
MOD_GlcNHglycan	336	339	PF01048	0.591
MOD_GlcNHglycan	346	349	PF01048	0.563
MOD_GlcNHglycan	362	365	PF01048	0.744
MOD_GlcNHglycan	381	384	PF01048	0.634
MOD_GlcNHglycan	387	390	PF01048	0.606
MOD_GlcNHglycan	442	445	PF01048	0.509
MOD_GlcNHglycan	507	510	PF01048	0.511
MOD_GlcNHglycan	531	534	PF01048	0.699
MOD_GlcNHglycan	55	58	PF01048	0.524
MOD_GlcNHglycan	875	878	PF01048	0.587
MOD_GlcNHglycan	914	917	PF01048	0.680
MOD_GlcNHglycan	927	931	PF01048	0.586
MOD_GlcNHglycan	944	948	PF01048	0.596
MOD_GlcNHglycan	965	968	PF01048	0.733
MOD_GlcNHglycan	974	977	PF01048	0.581
MOD_GlcNHglycan	978	981	PF01048	0.525
MOD_GlcNHglycan	991	994	PF01048	0.498
MOD_GSK3_1	1	8	PF00069	0.544
MOD_GSK3_1	1033	1040	PF00069	0.685
MOD_GSK3_1	12	19	PF00069	0.515
MOD_GSK3_1	182	189	PF00069	0.579
MOD_GSK3_1	240	247	PF00069	0.675
MOD_GSK3_1	253	260	PF00069	0.598
MOD_GSK3_1	289	296	PF00069	0.730
MOD_GSK3_1	340	347	PF00069	0.762
MOD_GSK3_1	381	388	PF00069	0.750
MOD_GSK3_1	391	398	PF00069	0.688
MOD_GSK3_1	501	508	PF00069	0.504
MOD_GSK3_1	525	532	PF00069	0.667
MOD_GSK3_1	53	60	PF00069	0.535
MOD_GSK3_1	635	642	PF00069	0.449
MOD_GSK3_1	778	785	PF00069	0.595
MOD_GSK3_1	817	824	PF00069	0.576
MOD_GSK3_1	848	855	PF00069	0.527
MOD_GSK3_1	866	873	PF00069	0.496
MOD_GSK3_1	91	98	PF00069	0.454
MOD_GSK3_1	963	970	PF00069	0.678
MOD_GSK3_1	972	979	PF00069	0.638
MOD_GSK3_1	985	992	PF00069	0.527
MOD_N-GLC_1	244	249	PF02516	0.707
MOD_N-GLC_1	391	396	PF02516	0.750
MOD_N-GLC_1	699	704	PF02516	0.385
MOD_N-GLC_1	803	808	PF02516	0.490
MOD_N-GLC_1	866	871	PF02516	0.614
MOD_N-GLC_1	970	975	PF02516	0.652
MOD_NEK2_1	1	6	PF00069	0.565
MOD_NEK2_1	1001	1006	PF00069	0.525
MOD_NEK2_1	169	174	PF00069	0.589
MOD_NEK2_1	257	262	PF00069	0.656
MOD_NEK2_1	583	588	PF00069	0.518
MOD_NEK2_1	634	639	PF00069	0.453
MOD_PIKK_1	1058	1064	PF00454	0.535
MOD_PIKK_1	183	189	PF00454	0.642
MOD_PIKK_1	244	250	PF00454	0.638
MOD_PIKK_1	583	589	PF00454	0.523
MOD_PKA_2	169	175	PF00069	0.598
MOD_PKA_2	215	221	PF00069	0.594
MOD_PKA_2	53	59	PF00069	0.527
MOD_PKA_2	675	681	PF00069	0.460
MOD_PKA_2	843	849	PF00069	0.512
MOD_PKA_2	851	857	PF00069	0.547
MOD_PKB_1	438	446	PF00069	0.512
MOD_Plk_1	252	258	PF00069	0.608
MOD_Plk_1	803	809	PF00069	0.492
MOD_Plk_1	85	91	PF00069	0.612
MOD_Plk_1	866	872	PF00069	0.611
MOD_Plk_1	970	976	PF00069	0.646
MOD_Plk_4	225	231	PF00069	0.510
MOD_Plk_4	424	430	PF00069	0.543
MOD_Plk_4	442	448	PF00069	0.444
MOD_Plk_4	639	645	PF00069	0.458
MOD_Plk_4	79	85	PF00069	0.615
MOD_Plk_4	855	861	PF00069	0.600
MOD_Plk_4	866	872	PF00069	0.533
MOD_Plk_4	91	97	PF00069	0.485
MOD_ProDKin_1	108	114	PF00069	0.556
MOD_ProDKin_1	133	139	PF00069	0.610
MOD_ProDKin_1	2	8	PF00069	0.555
MOD_ProDKin_1	33	39	PF00069	0.562
MOD_ProDKin_1	391	397	PF00069	0.701
MOD_ProDKin_1	44	50	PF00069	0.558
MOD_ProDKin_1	501	507	PF00069	0.505
MOD_ProDKin_1	525	531	PF00069	0.674
MOD_ProDKin_1	544	550	PF00069	0.806
MOD_ProDKin_1	556	562	PF00069	0.583
MOD_ProDKin_1	578	584	PF00069	0.497
MOD_ProDKin_1	784	790	PF00069	0.660
MOD_ProDKin_1	817	823	PF00069	0.517
MOD_ProDKin_1	859	865	PF00069	0.636
MOD_ProDKin_1	870	876	PF00069	0.514
MOD_ProDKin_1	95	101	PF00069	0.507
TRG_DiLeu_BaEn_1	496	501	PF01217	0.485
TRG_DiLeu_BaEn_1	572	577	PF01217	0.455
TRG_DiLeu_BaEn_1	686	691	PF01217	0.385
TRG_DiLeu_BaEn_1	73	78	PF01217	0.535
TRG_DiLeu_BaEn_2	441	447	PF01217	0.501
TRG_DiLeu_BaLyEn_6	452	457	PF01217	0.494
TRG_ENDOCYTIC_2	114	117	PF00928	0.497
TRG_ENDOCYTIC_2	230	233	PF00928	0.524
TRG_ENDOCYTIC_2	606	609	PF00928	0.466
TRG_ENDOCYTIC_2	616	619	PF00928	0.364
TRG_ENDOCYTIC_2	623	626	PF00928	0.258
TRG_ENDOCYTIC_2	660	663	PF00928	0.431
TRG_ENDOCYTIC_2	695	698	PF00928	0.385
TRG_ENDOCYTIC_2	729	732	PF00928	0.447
TRG_ENDOCYTIC_2	856	859	PF00928	0.535
TRG_ER_diArg_1	1002	1005	PF00400	0.527
TRG_ER_diArg_1	437	440	PF00400	0.524
TRG_ER_diArg_1	510	513	PF00400	0.519
TRG_ER_diArg_1	596	599	PF00400	0.518
TRG_ER_diArg_1	794	796	PF00400	0.468
TRG_ER_diArg_1	958	960	PF00400	0.700
TRG_NES_CRM1_1	482	496	PF08389	0.434

Homologs


Protein	Taxonomy	Sequence identity	Coverage
A0A3S5H6L1	Leishmania donovani	90%	100%
A4H6X4	Leishmania braziliensis	77%	100%
E9AGE8	Leishmania infantum	90%	100%
Q4QGN2	Leishmania major	91%	100%