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 major

UniProt:

Q4QGN2_LEIMA

TriTrypDb:

LmjF.12.0610 , LMJLV39_120011600 , LMJSD75_120011500

Length:

1025

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: 6
NetGPI	no	yes: 0, no: 6

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

Expansion

Sequence features

Q4QGN2

Sequence

MSA

Disorder

Secondary

Topology

Domains

SignalP

GPI

Phosphorylations

ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: Q4QGN2

Function

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

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	0.751
CLV_NRD_NRD_1	10	12	PF00675	0.653
CLV_NRD_NRD_1	743	745	PF00675	0.492
CLV_NRD_NRD_1	907	909	PF00675	0.739
CLV_PCSK_KEX2_1	10	12	PF00082	0.625
CLV_PCSK_KEX2_1	270	272	PF00082	0.832
CLV_PCSK_KEX2_1	578	580	PF00082	0.502
CLV_PCSK_KEX2_1	743	745	PF00082	0.492
CLV_PCSK_KEX2_1	906	908	PF00082	0.748
CLV_PCSK_PC1ET2_1	270	272	PF00082	0.832
CLV_PCSK_PC1ET2_1	578	580	PF00082	0.502
CLV_PCSK_SKI1_1	11	15	PF00082	0.536
CLV_PCSK_SKI1_1	438	442	PF00082	0.482
CLV_PCSK_SKI1_1	617	621	PF00082	0.462
CLV_PCSK_SKI1_1	744	748	PF00082	0.475
CLV_PCSK_SKI1_1	831	835	PF00082	0.694
CLV_PCSK_SKI1_1	86	90	PF00082	0.517
CLV_Separin_Metazoa	107	111	PF03568	0.702
CLV_Separin_Metazoa	150	154	PF03568	0.689
DEG_APCC_DBOX_1	580	588	PF00400	0.478
DEG_Nend_UBRbox_2	1	3	PF02207	0.649
DEG_SCF_FBW7_1	441	448	PF00400	0.567
DEG_SPOP_SBC_1	192	196	PF00917	0.660
DEG_SPOP_SBC_1	272	276	PF00917	0.816
DEG_SPOP_SBC_1	288	292	PF00917	0.538
DEG_SPOP_SBC_1	479	483	PF00917	0.797
DEG_SPOP_SBC_1	799	803	PF00917	0.625
DEG_SPOP_SBC_1	993	997	PF00917	0.688
DOC_ANK_TNKS_1	791	798	PF00023	0.561
DOC_CDC14_PxL_1	25	33	PF14671	0.767
DOC_CKS1_1	32	37	PF01111	0.582
DOC_CKS1_1	527	532	PF01111	0.489
DOC_CYCLIN_yCln2_LP_2	32	38	PF00134	0.778
DOC_CYCLIN_yCln2_LP_2	496	499	PF00134	0.599
DOC_CYCLIN_yCln2_LP_2	778	784	PF00134	0.483
DOC_MAPK_DCC_7	156	166	PF00069	0.577
DOC_MAPK_gen_1	578	584	PF00069	0.493
DOC_PP2B_LxvP_1	144	147	PF13499	0.731
DOC_PP2B_LxvP_1	228	231	PF13499	0.840
DOC_PP2B_LxvP_1	496	499	PF13499	0.599
DOC_PP2B_LxvP_1	778	781	PF13499	0.488
DOC_PP2B_LxvP_1	859	862	PF13499	0.625
DOC_USP7_MATH_1	1015	1019	PF00917	0.728
DOC_USP7_MATH_1	113	117	PF00917	0.741
DOC_USP7_MATH_1	121	125	PF00917	0.657
DOC_USP7_MATH_1	192	196	PF00917	0.843
DOC_USP7_MATH_1	27	31	PF00917	0.649
DOC_USP7_MATH_1	300	304	PF00917	0.724
DOC_USP7_MATH_1	325	329	PF00917	0.668
DOC_USP7_MATH_1	389	393	PF00917	0.604
DOC_USP7_MATH_1	445	449	PF00917	0.573
DOC_USP7_MATH_1	456	460	PF00917	0.660
DOC_USP7_MATH_1	751	755	PF00917	0.494
DOC_USP7_MATH_1	769	773	PF00917	0.614
DOC_USP7_MATH_1	791	795	PF00917	0.517
DOC_USP7_MATH_1	799	803	PF00917	0.640
DOC_USP7_MATH_1	877	881	PF00917	0.721
DOC_USP7_MATH_1	883	887	PF00917	0.682
DOC_USP7_MATH_1	918	922	PF00917	0.783
DOC_USP7_MATH_1	924	928	PF00917	0.694
DOC_USP7_MATH_1	972	976	PF00917	0.718
DOC_USP7_MATH_1	983	987	PF00917	0.696
DOC_USP7_MATH_1	993	997	PF00917	0.765
DOC_WW_Pin1_4	31	36	PF00397	0.580
DOC_WW_Pin1_4	318	323	PF00397	0.673
DOC_WW_Pin1_4	331	336	PF00397	0.623
DOC_WW_Pin1_4	441	446	PF00397	0.562
DOC_WW_Pin1_4	465	470	PF00397	0.788
DOC_WW_Pin1_4	48	53	PF00397	0.692
DOC_WW_Pin1_4	491	496	PF00397	0.796
DOC_WW_Pin1_4	504	509	PF00397	0.589
DOC_WW_Pin1_4	526	531	PF00397	0.600
DOC_WW_Pin1_4	73	78	PF00397	0.646
DOC_WW_Pin1_4	732	737	PF00397	0.559
DOC_WW_Pin1_4	765	770	PF00397	0.522
DOC_WW_Pin1_4	807	812	PF00397	0.671
DOC_WW_Pin1_4	818	823	PF00397	0.663
DOC_WW_Pin1_4	873	878	PF00397	0.768
LIG_14-3-3_CanoR_1	153	163	PF00244	0.615
LIG_14-3-3_CanoR_1	271	281	PF00244	0.814
LIG_14-3-3_CanoR_1	581	591	PF00244	0.478
LIG_14-3-3_CanoR_1	624	630	PF00244	0.587
LIG_14-3-3_CanoR_1	790	796	PF00244	0.626
LIG_14-3-3_CanoR_1	800	805	PF00244	0.584
LIG_Actin_WH2_2	384	400	PF00022	0.497
LIG_Actin_WH2_2	436	454	PF00022	0.564
LIG_APCC_ABBAyCdc20_2	757	763	PF00400	0.585
LIG_BRCT_BRCA1_1	326	330	PF00533	0.790
LIG_BRCT_BRCA1_1	382	386	PF00533	0.612
LIG_BRCT_BRCA1_1	461	465	PF00533	0.724
LIG_BRCT_BRCA1_1	522	526	PF00533	0.605
LIG_BRCT_BRCA1_1	60	64	PF00533	0.777
LIG_Clathr_ClatBox_1	359	363	PF01394	0.610
LIG_EH_1	1013	1017	PF12763	0.587
LIG_EVH1_2	945	949	PF00568	0.712
LIG_FHA_1	155	161	PF00498	0.625
LIG_FHA_1	292	298	PF00498	0.721
LIG_FHA_1	354	360	PF00498	0.781
LIG_FHA_1	383	389	PF00498	0.496
LIG_FHA_1	491	497	PF00498	0.731
LIG_FHA_1	505	511	PF00498	0.712
LIG_FHA_1	648	654	PF00498	0.369
LIG_FHA_1	691	697	PF00498	0.478
LIG_FHA_1	745	751	PF00498	0.578
LIG_FHA_1	771	777	PF00498	0.606
LIG_FHA_1	976	982	PF00498	0.614
LIG_FHA_2	575	581	PF00498	0.493
LIG_FHA_2	624	630	PF00498	0.587
LIG_FHA_2	656	662	PF00498	0.513
LIG_FHA_2	853	859	PF00498	0.672
LIG_LIR_Apic_2	129	133	PF02991	0.649
LIG_LIR_Gen_1	168	177	PF02991	0.656
LIG_LIR_Gen_1	327	336	PF02991	0.717
LIG_LIR_Gen_1	516	527	PF02991	0.466
LIG_LIR_Gen_1	551	562	PF02991	0.502
LIG_LIR_Gen_1	570	576	PF02991	0.449
LIG_LIR_Gen_1	634	644	PF02991	0.411
LIG_LIR_Gen_1	78	89	PF02991	0.614
LIG_LIR_Gen_1	801	811	PF02991	0.573
LIG_LIR_Nem_3	168	173	PF02991	0.646
LIG_LIR_Nem_3	327	333	PF02991	0.714
LIG_LIR_Nem_3	425	430	PF02991	0.565
LIG_LIR_Nem_3	48	53	PF02991	0.757
LIG_LIR_Nem_3	516	522	PF02991	0.436
LIG_LIR_Nem_3	551	557	PF02991	0.460
LIG_LIR_Nem_3	561	567	PF02991	0.401
LIG_LIR_Nem_3	570	574	PF02991	0.444
LIG_LIR_Nem_3	634	639	PF02991	0.411
LIG_LIR_Nem_3	735	741	PF02991	0.519
LIG_LIR_Nem_3	78	84	PF02991	0.713
LIG_LIR_Nem_3	801	807	PF02991	0.563
LIG_MYND_1	495	499	PF01753	0.600
LIG_PCNA_TLS_4	86	94	PF02747	0.567
LIG_PCNA_yPIPBox_3	598	609	PF02747	0.447
LIG_Pex14_2	522	526	PF04695	0.605
LIG_PTB_Apo_2	570	577	PF02174	0.455
LIG_PTB_Apo_2	749	756	PF02174	0.503
LIG_PTB_Phospho_1	570	576	PF10480	0.449
LIG_PTB_Phospho_1	749	755	PF10480	0.602
LIG_Rb_LxCxE_1	719	737	PF01857	0.514
LIG_Rb_pABgroove_1	563	571	PF01858	0.578
LIG_SH2_CRK	554	558	PF00017	0.487
LIG_SH2_CRK	571	575	PF00017	0.438
LIG_SH2_CRK	804	808	PF00017	0.671
LIG_SH2_GRB2like	571	574	PF00017	0.439
LIG_SH2_PTP2	609	612	PF00017	0.461
LIG_SH2_PTP2	643	646	PF00017	0.411
LIG_SH2_SRC	569	572	PF00017	0.450
LIG_SH2_SRC	643	646	PF00017	0.411
LIG_SH2_STAP1	170	174	PF00017	0.552
LIG_SH2_STAP1	571	575	PF00017	0.438
LIG_SH2_STAP1	804	808	PF00017	0.593
LIG_SH2_STAT3	540	543	PF00017	0.500
LIG_SH2_STAT5	216	219	PF00017	0.611
LIG_SH2_STAT5	365	368	PF00017	0.500
LIG_SH2_STAT5	564	567	PF00017	0.554
LIG_SH2_STAT5	576	579	PF00017	0.401
LIG_SH2_STAT5	609	612	PF00017	0.461
LIG_SH2_STAT5	643	646	PF00017	0.381
LIG_SH2_STAT5	741	744	PF00017	0.490
LIG_SH2_STAT5	755	758	PF00017	0.504
LIG_SH2_STAT5	761	764	PF00017	0.443
LIG_SH2_STAT5	787	790	PF00017	0.446
LIG_SH2_STAT5	91	94	PF00017	0.511
LIG_SH3_1	492	498	PF00018	0.638
LIG_SH3_3	117	123	PF00018	0.696
LIG_SH3_3	464	470	PF00018	0.799
LIG_SH3_3	492	498	PF00018	0.749
LIG_SH3_3	505	511	PF00018	0.769
LIG_SH3_3	524	530	PF00018	0.401
LIG_SH3_3	695	701	PF00018	0.493
LIG_SH3_3	733	739	PF00018	0.541
LIG_Sin3_3	635	642	PF02671	0.411
LIG_TYR_ITAM	551	567	PF00017	0.598
LIG_WW_3	498	502	PF00397	0.753
MOD_CDK_SPxxK_3	335	342	PF00069	0.719
MOD_CDK_SPxxK_3	48	55	PF00069	0.548
MOD_CK1_1	21	27	PF00069	0.599
MOD_CK1_1	233	239	PF00069	0.801
MOD_CK1_1	287	293	PF00069	0.737
MOD_CK1_1	321	327	PF00069	0.679
MOD_CK1_1	328	334	PF00069	0.672
MOD_CK1_1	409	415	PF00069	0.453
MOD_CK1_1	459	465	PF00069	0.714
MOD_CK1_1	48	54	PF00069	0.663
MOD_CK1_1	732	738	PF00069	0.652
MOD_CK1_1	75	81	PF00069	0.539
MOD_CK1_1	753	759	PF00069	0.443
MOD_CK1_1	803	809	PF00069	0.652
MOD_CK1_1	817	823	PF00069	0.643
MOD_CK1_1	975	981	PF00069	0.592
MOD_CK1_1	988	994	PF00069	0.730
MOD_CK1_1	995	1001	PF00069	0.831
MOD_CK2_1	233	239	PF00069	0.787
MOD_CK2_1	655	661	PF00069	0.429
MOD_CK2_1	790	796	PF00069	0.537
MOD_CK2_1	852	858	PF00069	0.662
MOD_GlcNHglycan	267	270	PF01048	0.760
MOD_GlcNHglycan	276	279	PF01048	0.620
MOD_GlcNHglycan	286	289	PF01048	0.600
MOD_GlcNHglycan	302	305	PF01048	0.694
MOD_GlcNHglycan	382	385	PF01048	0.544
MOD_GlcNHglycan	447	450	PF01048	0.697
MOD_GlcNHglycan	458	461	PF01048	0.592
MOD_GlcNHglycan	471	474	PF01048	0.755
MOD_GlcNHglycan	60	63	PF01048	0.734
MOD_GlcNHglycan	77	80	PF01048	0.680
MOD_GlcNHglycan	823	826	PF01048	0.629
MOD_GlcNHglycan	862	865	PF01048	0.807
MOD_GlcNHglycan	879	882	PF01048	0.608
MOD_GlcNHglycan	913	916	PF01048	0.802
MOD_GlcNHglycan	922	925	PF01048	0.639
MOD_GlcNHglycan	926	929	PF01048	0.518
MOD_GlcNHglycan	939	942	PF01048	0.533
MOD_GlcNHglycan	974	977	PF01048	0.619
MOD_GlcNHglycan	983	986	PF01048	0.684
MOD_GSK3_1	109	116	PF00069	0.645
MOD_GSK3_1	11	18	PF00069	0.600
MOD_GSK3_1	122	129	PF00069	0.745
MOD_GSK3_1	180	187	PF00069	0.752
MOD_GSK3_1	229	236	PF00069	0.759
MOD_GSK3_1	27	34	PF00069	0.676
MOD_GSK3_1	280	287	PF00069	0.747
MOD_GSK3_1	296	303	PF00069	0.693
MOD_GSK3_1	307	314	PF00069	0.666
MOD_GSK3_1	321	328	PF00069	0.717
MOD_GSK3_1	331	338	PF00069	0.634
MOD_GSK3_1	441	448	PF00069	0.567
MOD_GSK3_1	465	472	PF00069	0.812
MOD_GSK3_1	478	485	PF00069	0.840
MOD_GSK3_1	583	590	PF00069	0.572
MOD_GSK3_1	726	733	PF00069	0.578
MOD_GSK3_1	765	772	PF00069	0.634
MOD_GSK3_1	799	806	PF00069	0.629
MOD_GSK3_1	814	821	PF00069	0.600
MOD_GSK3_1	873	880	PF00069	0.690
MOD_GSK3_1	918	925	PF00069	0.724
MOD_GSK3_1	933	940	PF00069	0.527
MOD_GSK3_1	981	988	PF00069	0.711
MOD_GSK3_1	991	998	PF00069	0.753
MOD_N-GLC_1	184	189	PF02516	0.727
MOD_N-GLC_1	233	238	PF02516	0.699
MOD_N-GLC_1	331	336	PF02516	0.720
MOD_N-GLC_1	647	652	PF02516	0.411
MOD_N-GLC_1	751	756	PF02516	0.515
MOD_N-GLC_1	814	819	PF02516	0.718
MOD_N-GLC_1	918	923	PF02516	0.724
MOD_NEK2_1	109	114	PF00069	0.738
MOD_NEK2_1	155	160	PF00069	0.623
MOD_NEK2_1	531	536	PF00069	0.563
MOD_NEK2_1	582	587	PF00069	0.444
MOD_NEK2_1	798	803	PF00069	0.663
MOD_NEK2_1	949	954	PF00069	0.674
MOD_NEK2_2	325	330	PF00069	0.638
MOD_NEK2_2	45	50	PF00069	0.550
MOD_PIKK_1	1015	1021	PF00454	0.727
MOD_PIKK_1	123	129	PF00454	0.742
MOD_PIKK_1	184	190	PF00454	0.731
MOD_PIKK_1	409	415	PF00454	0.412
MOD_PIKK_1	531	537	PF00454	0.460
MOD_PIKK_1	988	994	PF00454	0.789
MOD_PIKK_1	995	1001	PF00454	0.672
MOD_PKA_1	906	912	PF00069	0.751
MOD_PKA_2	109	115	PF00069	0.744
MOD_PKA_2	155	161	PF00069	0.578
MOD_PKA_2	409	415	PF00069	0.412
MOD_PKA_2	623	629	PF00069	0.587
MOD_PKA_2	791	797	PF00069	0.634
MOD_PKA_2	799	805	PF00069	0.614
MOD_PKA_2	906	912	PF00069	0.867
MOD_PKB_1	378	386	PF00069	0.628
MOD_Plk_1	192	198	PF00069	0.661
MOD_Plk_1	21	27	PF00069	0.658
MOD_Plk_1	751	757	PF00069	0.516
MOD_Plk_1	814	820	PF00069	0.717
MOD_Plk_1	918	924	PF00069	0.714
MOD_Plk_4	15	21	PF00069	0.655
MOD_Plk_4	165	171	PF00069	0.613
MOD_Plk_4	27	33	PF00069	0.665
MOD_Plk_4	325	331	PF00069	0.700
MOD_Plk_4	364	370	PF00069	0.492
MOD_Plk_4	382	388	PF00069	0.326
MOD_Plk_4	45	51	PF00069	0.675
MOD_Plk_4	587	593	PF00069	0.431
MOD_Plk_4	803	809	PF00069	0.679
MOD_Plk_4	814	820	PF00069	0.767
MOD_ProDKin_1	31	37	PF00069	0.581
MOD_ProDKin_1	318	324	PF00069	0.673
MOD_ProDKin_1	331	337	PF00069	0.622
MOD_ProDKin_1	441	447	PF00069	0.562
MOD_ProDKin_1	465	471	PF00069	0.790
MOD_ProDKin_1	48	54	PF00069	0.694
MOD_ProDKin_1	491	497	PF00069	0.797
MOD_ProDKin_1	504	510	PF00069	0.581
MOD_ProDKin_1	526	532	PF00069	0.593
MOD_ProDKin_1	73	79	PF00069	0.638
MOD_ProDKin_1	732	738	PF00069	0.550
MOD_ProDKin_1	765	771	PF00069	0.521
MOD_ProDKin_1	807	813	PF00069	0.674
MOD_ProDKin_1	818	824	PF00069	0.660
MOD_ProDKin_1	873	879	PF00069	0.768
MOD_SUMO_for_1	93	96	PF00179	0.572
TRG_DiLeu_BaEn_1	436	441	PF01217	0.510
TRG_DiLeu_BaEn_1	520	525	PF01217	0.499
TRG_DiLeu_BaEn_1	634	639	PF01217	0.411
TRG_DiLeu_BaEn_2	381	387	PF01217	0.513
TRG_DiLeu_BaLyEn_6	159	164	PF01217	0.545
TRG_DiLeu_BaLyEn_6	392	397	PF01217	0.503
TRG_DiLeu_BaLyEn_6	492	497	PF01217	0.612
TRG_ENDOCYTIC_2	170	173	PF00928	0.550
TRG_ENDOCYTIC_2	554	557	PF00928	0.486
TRG_ENDOCYTIC_2	564	567	PF00928	0.481
TRG_ENDOCYTIC_2	571	574	PF00928	0.439
TRG_ENDOCYTIC_2	608	611	PF00928	0.456
TRG_ENDOCYTIC_2	643	646	PF00928	0.411
TRG_ENDOCYTIC_2	677	680	PF00928	0.469
TRG_ENDOCYTIC_2	804	807	PF00928	0.670
TRG_ER_diArg_1	377	380	PF00400	0.520
TRG_ER_diArg_1	450	453	PF00400	0.608
TRG_ER_diArg_1	544	547	PF00400	0.537
TRG_ER_diArg_1	742	744	PF00400	0.495
TRG_ER_diArg_1	906	908	PF00400	0.739
TRG_ER_diArg_1	950	953	PF00400	0.572
TRG_NES_CRM1_1	422	436	PF08389	0.527

Homologs


Protein	Taxonomy	Sequence identity	Coverage
A0A0N1PEG3	Leptomonas seymouri	55%	92%
A0A3S5H6L1	Leishmania donovani	91%	100%
A4H6X4	Leishmania braziliensis	80%	99%
E9AGE8	Leishmania infantum	91%	100%
E9ANY8	Leishmania mexicana (strain MHOM/GT/2001/U1103)	91%	96%