AAA domain-containing protein

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

Quick info

Protein:

Gene product:

AAA ATPase domain containing protein, putative

Species:

Leishmania mexicana

UniProt:

E9AYK1_LEIMU

TriTrypDb:

LmxM.26.2210

Length:

887

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: 7
NetGPI	no	yes: 0, no: 7

Cellular components
Term	Name	Level	Count
GO:0005634	nucleus	5	1
GO:0043226	organelle	2	1
GO:0043227	membrane-bounded organelle	3	1
GO:0043229	intracellular organelle	3	1
GO:0043231	intracellular membrane-bounded organelle	4	1
GO:0110165	cellular anatomical entity	1	1

Expansion

Sequence features

E9AYK1

Sequence

MSA

Disorder

Secondary

Topology

Domains

SignalP

GPI

Phosphorylations

ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: E9AYK1

Function

Biological processes
Term	Name	Level	Count
GO:0000075	cell cycle checkpoint signaling	4	1
GO:0000076	DNA replication checkpoint signaling	6	1
GO:0007093	mitotic cell cycle checkpoint signaling	4	1
GO:0007165	signal transduction	2	1
GO:0007346	regulation of mitotic cell cycle	5	1
GO:0009987	cellular process	1	1
GO:0010389	regulation of G2/M transition of mitotic cell cycle	7	1
GO:0010564	regulation of cell cycle process	5	1
GO:0010948	negative regulation of cell cycle process	6	1
GO:0010972	negative regulation of G2/M transition of mitotic cell cycle	8	1
GO:0022402	cell cycle process	2	1
GO:0031570	DNA integrity checkpoint signaling	5	1
GO:0033314	mitotic DNA replication checkpoint signaling	6	1
GO:0035556	intracellular signal transduction	3	1
GO:0044774	mitotic DNA integrity checkpoint signaling	5	1
GO:0044818	mitotic G2/M transition checkpoint	5	1
GO:0045786	negative regulation of cell cycle	5	1
GO:0045930	negative regulation of mitotic cell cycle	6	1
GO:0048519	negative regulation of biological process	3	1
GO:0048523	negative regulation of cellular process	4	1
GO:0050789	regulation of biological process	2	1
GO:0050794	regulation of cellular process	3	1
GO:0051726	regulation of cell cycle	4	1
GO:0065007	biological regulation	1	1
GO:1901987	regulation of cell cycle phase transition	6	1
GO:1901988	negative regulation of cell cycle phase transition	7	1
GO:1901990	regulation of mitotic cell cycle phase transition	6	1
GO:1901991	negative regulation of mitotic cell cycle phase transition	7	1
GO:1902749	regulation of cell cycle G2/M phase transition	7	1
GO:1902750	negative regulation of cell cycle G2/M phase transition	8	1
GO:1903047	mitotic cell cycle process	3	1

Molecular functions
Term	Name	Level	Count
GO:0003676	nucleic acid binding	3	1
GO:0003677	DNA binding	4	1
GO:0003688	DNA replication origin binding	7	1
GO:0003690	double-stranded DNA binding	5	1
GO:0005488	binding	1	1
GO:0043565	sequence-specific DNA binding	5	1
GO:0097159	organic cyclic compound binding	2	1
GO:1901363	heterocyclic compound binding	2	1
GO:1990837	sequence-specific double-stranded DNA binding	6	1

Putative motif mimicry


Leishmania	From	To	Domain/Motif	Score
CLV_C14_Caspase3-7	134	138	PF00656	0.478
CLV_C14_Caspase3-7	367	371	PF00656	0.513
CLV_C14_Caspase3-7	39	43	PF00656	0.601
CLV_C14_Caspase3-7	659	663	PF00656	0.625
CLV_NRD_NRD_1	13	15	PF00675	0.689
CLV_NRD_NRD_1	147	149	PF00675	0.801
CLV_NRD_NRD_1	249	251	PF00675	0.514
CLV_NRD_NRD_1	29	31	PF00675	0.553
CLV_NRD_NRD_1	412	414	PF00675	0.563
CLV_NRD_NRD_1	524	526	PF00675	0.698
CLV_NRD_NRD_1	555	557	PF00675	0.418
CLV_NRD_NRD_1	612	614	PF00675	0.542
CLV_NRD_NRD_1	72	74	PF00675	0.434
CLV_NRD_NRD_1	746	748	PF00675	0.442
CLV_PCSK_FUR_1	11	15	PF00082	0.642
CLV_PCSK_FUR_1	250	254	PF00082	0.581
CLV_PCSK_FUR_1	610	614	PF00082	0.502
CLV_PCSK_KEX2_1	13	15	PF00082	0.689
CLV_PCSK_KEX2_1	147	149	PF00082	0.692
CLV_PCSK_KEX2_1	249	251	PF00082	0.609
CLV_PCSK_KEX2_1	252	254	PF00082	0.622
CLV_PCSK_KEX2_1	29	31	PF00082	0.553
CLV_PCSK_KEX2_1	411	413	PF00082	0.582
CLV_PCSK_KEX2_1	612	614	PF00082	0.542
CLV_PCSK_KEX2_1	72	74	PF00082	0.434
CLV_PCSK_KEX2_1	853	855	PF00082	0.476
CLV_PCSK_KEX2_1	97	99	PF00082	0.388
CLV_PCSK_PC1ET2_1	252	254	PF00082	0.623
CLV_PCSK_PC1ET2_1	411	413	PF00082	0.582
CLV_PCSK_PC1ET2_1	853	855	PF00082	0.476
CLV_PCSK_PC1ET2_1	97	99	PF00082	0.438
CLV_PCSK_SKI1_1	219	223	PF00082	0.652
CLV_PCSK_SKI1_1	249	253	PF00082	0.591
CLV_PCSK_SKI1_1	337	341	PF00082	0.495
CLV_PCSK_SKI1_1	436	440	PF00082	0.465
CLV_PCSK_SKI1_1	516	520	PF00082	0.516
CLV_PCSK_SKI1_1	556	560	PF00082	0.388
CLV_PCSK_SKI1_1	72	76	PF00082	0.419
CLV_PCSK_SKI1_1	97	101	PF00082	0.432
CLV_Separin_Metazoa	877	881	PF03568	0.419
DEG_SCF_FBW7_1	153	160	PF00400	0.706
DEG_SCF_FBW7_1	181	186	PF00400	0.685
DEG_SPOP_SBC_1	183	187	PF00917	0.549
DEG_SPOP_SBC_1	235	239	PF00917	0.520
DEG_SPOP_SBC_1	403	407	PF00917	0.587
DEG_SPOP_SBC_1	600	604	PF00917	0.552
DEG_SPOP_SBC_1	666	670	PF00917	0.567
DOC_CKS1_1	154	159	PF01111	0.699
DOC_CYCLIN_RxL_1	554	563	PF00134	0.448
DOC_CYCLIN_RxL_1	69	78	PF00134	0.326
DOC_MAPK_DCC_7	411	421	PF00069	0.519
DOC_MAPK_gen_1	537	546	PF00069	0.476
DOC_MAPK_gen_1	556	562	PF00069	0.532
DOC_MAPK_HePTP_8	775	787	PF00069	0.379
DOC_MAPK_MEF2A_6	412	421	PF00069	0.511
DOC_MAPK_MEF2A_6	778	787	PF00069	0.520
DOC_PP1_RVXF_1	798	804	PF00149	0.488
DOC_PP4_FxxP_1	446	449	PF00568	0.439
DOC_USP7_MATH_1	161	165	PF00917	0.695
DOC_USP7_MATH_1	183	187	PF00917	0.667
DOC_USP7_MATH_1	199	203	PF00917	0.705
DOC_USP7_MATH_1	206	210	PF00917	0.643
DOC_USP7_MATH_1	214	218	PF00917	0.746
DOC_USP7_MATH_1	225	229	PF00917	0.684
DOC_USP7_MATH_1	230	234	PF00917	0.661
DOC_USP7_MATH_1	326	330	PF00917	0.723
DOC_USP7_MATH_1	331	335	PF00917	0.599
DOC_USP7_MATH_1	347	351	PF00917	0.293
DOC_USP7_MATH_1	364	368	PF00917	0.329
DOC_USP7_MATH_1	386	390	PF00917	0.573
DOC_USP7_MATH_1	398	402	PF00917	0.464
DOC_USP7_MATH_1	404	408	PF00917	0.760
DOC_USP7_MATH_1	514	518	PF00917	0.582
DOC_USP7_MATH_1	528	532	PF00917	0.588
DOC_USP7_MATH_1	600	604	PF00917	0.552
DOC_USP7_MATH_1	606	610	PF00917	0.699
DOC_USP7_MATH_1	678	682	PF00917	0.672
DOC_USP7_MATH_1	68	72	PF00917	0.448
DOC_USP7_MATH_1	693	697	PF00917	0.667
DOC_USP7_MATH_1	755	759	PF00917	0.489
DOC_WW_Pin1_4	153	158	PF00397	0.713
DOC_WW_Pin1_4	171	176	PF00397	0.595
DOC_WW_Pin1_4	179	184	PF00397	0.611
DOC_WW_Pin1_4	19	24	PF00397	0.756
DOC_WW_Pin1_4	195	200	PF00397	0.698
DOC_WW_Pin1_4	221	226	PF00397	0.688
DOC_WW_Pin1_4	243	248	PF00397	0.696
DOC_WW_Pin1_4	324	329	PF00397	0.681
DOC_WW_Pin1_4	412	417	PF00397	0.543
DOC_WW_Pin1_4	509	514	PF00397	0.620
DOC_WW_Pin1_4	601	606	PF00397	0.612
DOC_WW_Pin1_4	696	701	PF00397	0.634
DOC_WW_Pin1_4	765	770	PF00397	0.636
LIG_14-3-3_CanoR_1	101	109	PF00244	0.425
LIG_14-3-3_CanoR_1	148	154	PF00244	0.669
LIG_14-3-3_CanoR_1	323	331	PF00244	0.622
LIG_14-3-3_CanoR_1	530	539	PF00244	0.653
LIG_14-3-3_CanoR_1	540	548	PF00244	0.441
LIG_14-3-3_CanoR_1	575	580	PF00244	0.436
LIG_14-3-3_CanoR_1	612	618	PF00244	0.599
LIG_14-3-3_CanoR_1	648	654	PF00244	0.541
LIG_14-3-3_CanoR_1	658	666	PF00244	0.737
LIG_14-3-3_CanoR_1	834	839	PF00244	0.447
LIG_14-3-3_CanoR_1	862	870	PF00244	0.536
LIG_Actin_WH2_2	415	433	PF00022	0.452
LIG_Actin_WH2_2	817	832	PF00022	0.467
LIG_APCC_ABBA_1	476	481	PF00400	0.451
LIG_BIR_III_4	177	181	PF00653	0.686
LIG_BIR_III_4	662	666	PF00653	0.638
LIG_EH1_1	44	52	PF00400	0.539
LIG_eIF4E_1	69	75	PF01652	0.318
LIG_FHA_1	236	242	PF00498	0.779
LIG_FHA_1	273	279	PF00498	0.704
LIG_FHA_1	371	377	PF00498	0.368
LIG_FHA_1	613	619	PF00498	0.677
LIG_FHA_1	732	738	PF00498	0.392
LIG_FHA_1	780	786	PF00498	0.454
LIG_FHA_1	830	836	PF00498	0.437
LIG_FHA_1	839	845	PF00498	0.396
LIG_FHA_1	91	97	PF00498	0.382
LIG_FHA_2	120	126	PF00498	0.627
LIG_FHA_2	128	134	PF00498	0.586
LIG_FHA_2	195	201	PF00498	0.696
LIG_FHA_2	238	244	PF00498	0.692
LIG_FHA_2	277	283	PF00498	0.605
LIG_FHA_2	47	53	PF00498	0.563
LIG_FHA_2	490	496	PF00498	0.462
LIG_FHA_2	727	733	PF00498	0.450
LIG_LIR_Apic_2	443	449	PF02991	0.384
LIG_LIR_Apic_2	841	845	PF02991	0.487
LIG_LIR_Gen_1	315	324	PF02991	0.394
LIG_LIR_Gen_1	60	70	PF02991	0.406
LIG_LIR_Gen_1	872	883	PF02991	0.432
LIG_LIR_Nem_3	310	316	PF02991	0.429
LIG_LIR_Nem_3	333	339	PF02991	0.524
LIG_LIR_Nem_3	578	584	PF02991	0.451
LIG_LIR_Nem_3	60	66	PF02991	0.418
LIG_LIR_Nem_3	820	824	PF02991	0.405
LIG_LIR_Nem_3	872	878	PF02991	0.440
LIG_LYPXL_yS_3	313	316	PF13949	0.443
LIG_NRBOX	881	887	PF00104	0.326
LIG_PCNA_PIPBox_1	787	796	PF02747	0.457
LIG_Pex14_2	336	340	PF04695	0.434
LIG_RPA_C_Fungi	583	595	PF08784	0.325
LIG_SH2_CRK	551	555	PF00017	0.414
LIG_SH2_CRK	794	798	PF00017	0.372
LIG_SH2_GRB2like	343	346	PF00017	0.357
LIG_SH2_NCK_1	304	308	PF00017	0.486
LIG_SH2_NCK_1	479	483	PF00017	0.416
LIG_SH2_SRC	551	554	PF00017	0.418
LIG_SH2_STAP1	304	308	PF00017	0.486
LIG_SH2_STAP1	551	555	PF00017	0.414
LIG_SH2_STAP1	63	67	PF00017	0.441
LIG_SH2_STAP1	794	798	PF00017	0.372
LIG_SH2_STAT5	308	311	PF00017	0.491
LIG_SH2_STAT5	343	346	PF00017	0.357
LIG_SH2_STAT5	429	432	PF00017	0.413
LIG_SH2_STAT5	553	556	PF00017	0.363
LIG_SH2_STAT5	69	72	PF00017	0.344
LIG_SH2_STAT5	736	739	PF00017	0.392
LIG_SH2_STAT5	794	797	PF00017	0.376
LIG_SH3_1	151	157	PF00018	0.634
LIG_SH3_3	151	157	PF00018	0.624
LIG_SH3_3	293	299	PF00018	0.598
LIG_SH3_3	325	331	PF00018	0.601
LIG_SH3_3	346	352	PF00018	0.417
LIG_SH3_3	35	41	PF00018	0.604
LIG_SH3_3	461	467	PF00018	0.398
LIG_SH3_3	687	693	PF00018	0.597
LIG_SUMO_SIM_anti_2	739	745	PF11976	0.343
LIG_SUMO_SIM_par_1	350	356	PF11976	0.446
LIG_SUMO_SIM_par_1	420	426	PF11976	0.347
LIG_SUMO_SIM_par_1	739	745	PF11976	0.403
LIG_TRAF2_1	122	125	PF00917	0.726
LIG_TRAF2_1	168	171	PF00917	0.705
LIG_UBA3_1	376	385	PF00899	0.451
LIG_WW_3	295	299	PF00397	0.591
MOD_CDC14_SPxK_1	246	249	PF00782	0.548
MOD_CDK_SPK_2	157	162	PF00069	0.688
MOD_CDK_SPxK_1	243	249	PF00069	0.551
MOD_CDK_SPxxK_3	19	26	PF00069	0.595
MOD_CDK_SPxxK_3	243	250	PF00069	0.577
MOD_CDK_SPxxK_3	509	516	PF00069	0.539
MOD_CK1_1	184	190	PF00069	0.685
MOD_CK1_1	194	200	PF00069	0.709
MOD_CK1_1	202	208	PF00069	0.787
MOD_CK1_1	21	27	PF00069	0.634
MOD_CK1_1	224	230	PF00069	0.672
MOD_CK1_1	231	237	PF00069	0.711
MOD_CK1_1	264	270	PF00069	0.635
MOD_CK1_1	28	34	PF00069	0.641
MOD_CK1_1	319	325	PF00069	0.696
MOD_CK1_1	327	333	PF00069	0.620
MOD_CK1_1	405	411	PF00069	0.717
MOD_CK1_1	531	537	PF00069	0.496
MOD_CK1_1	654	660	PF00069	0.667
MOD_CK1_1	668	674	PF00069	0.536
MOD_CK1_1	696	702	PF00069	0.700
MOD_CK2_1	118	124	PF00069	0.646
MOD_CK2_1	127	133	PF00069	0.686
MOD_CK2_1	237	243	PF00069	0.805
MOD_CK2_1	276	282	PF00069	0.611
MOD_CK2_1	46	52	PF00069	0.558
MOD_CK2_1	489	495	PF00069	0.466
MOD_CK2_1	625	631	PF00069	0.570
MOD_CK2_1	726	732	PF00069	0.455
MOD_GlcNHglycan	103	106	PF01048	0.459
MOD_GlcNHglycan	204	207	PF01048	0.799
MOD_GlcNHglycan	208	211	PF01048	0.738
MOD_GlcNHglycan	216	219	PF01048	0.489
MOD_GlcNHglycan	266	269	PF01048	0.712
MOD_GlcNHglycan	282	285	PF01048	0.542
MOD_GlcNHglycan	3	6	PF01048	0.790
MOD_GlcNHglycan	30	33	PF01048	0.701
MOD_GlcNHglycan	348	352	PF01048	0.417
MOD_GlcNHglycan	407	410	PF01048	0.562
MOD_GlcNHglycan	489	492	PF01048	0.438
MOD_GlcNHglycan	516	519	PF01048	0.740
MOD_GlcNHglycan	520	523	PF01048	0.605
MOD_GlcNHglycan	531	534	PF01048	0.629
MOD_GlcNHglycan	561	565	PF01048	0.417
MOD_GlcNHglycan	621	624	PF01048	0.499
MOD_GlcNHglycan	653	656	PF01048	0.753
MOD_GlcNHglycan	659	662	PF01048	0.684
MOD_GlcNHglycan	674	677	PF01048	0.655
MOD_GlcNHglycan	695	698	PF01048	0.623
MOD_GlcNHglycan	701	704	PF01048	0.571
MOD_GSK3_1	133	140	PF00069	0.795
MOD_GSK3_1	149	156	PF00069	0.663
MOD_GSK3_1	157	164	PF00069	0.611
MOD_GSK3_1	179	186	PF00069	0.803
MOD_GSK3_1	191	198	PF00069	0.731
MOD_GSK3_1	201	208	PF00069	0.685
MOD_GSK3_1	21	28	PF00069	0.820
MOD_GSK3_1	210	217	PF00069	0.548
MOD_GSK3_1	221	228	PF00069	0.587
MOD_GSK3_1	230	237	PF00069	0.727
MOD_GSK3_1	272	279	PF00069	0.709
MOD_GSK3_1	315	322	PF00069	0.677
MOD_GSK3_1	326	333	PF00069	0.561
MOD_GSK3_1	358	365	PF00069	0.389
MOD_GSK3_1	366	373	PF00069	0.423
MOD_GSK3_1	398	405	PF00069	0.618
MOD_GSK3_1	514	521	PF00069	0.643
MOD_GSK3_1	524	531	PF00069	0.709
MOD_GSK3_1	596	603	PF00069	0.639
MOD_GSK3_1	644	651	PF00069	0.616
MOD_GSK3_1	653	660	PF00069	0.599
MOD_GSK3_1	665	672	PF00069	0.566
MOD_GSK3_1	695	702	PF00069	0.590
MOD_GSK3_1	703	710	PF00069	0.421
MOD_GSK3_1	834	841	PF00069	0.407
MOD_N-GLC_1	235	240	PF02516	0.651
MOD_N-GLC_1	619	624	PF02516	0.617
MOD_N-GLC_1	666	671	PF02516	0.493
MOD_N-GLC_1	78	83	PF02516	0.433
MOD_N-GLC_1	838	843	PF02516	0.422
MOD_NEK2_1	193	198	PF00069	0.691
MOD_NEK2_1	316	321	PF00069	0.522
MOD_NEK2_1	653	658	PF00069	0.573
MOD_NEK2_1	707	712	PF00069	0.449
MOD_NEK2_1	75	80	PF00069	0.370
MOD_NEK2_1	838	843	PF00069	0.422
MOD_NEK2_2	307	312	PF00069	0.447
MOD_NEK2_2	731	736	PF00069	0.434
MOD_NEK2_2	781	786	PF00069	0.488
MOD_OFUCOSY	126	131	PF10250	0.531
MOD_OFUCOSY	359	366	PF10250	0.445
MOD_PIKK_1	21	27	PF00454	0.661
MOD_PIKK_1	331	337	PF00454	0.538
MOD_PIKK_1	370	376	PF00454	0.475
MOD_PK_1	36	42	PF00069	0.559
MOD_PK_1	575	581	PF00069	0.397
MOD_PKA_1	612	618	PF00069	0.496
MOD_PKA_2	146	152	PF00069	0.756
MOD_PKA_2	161	167	PF00069	0.688
MOD_PKA_2	202	208	PF00069	0.690
MOD_PKA_2	228	234	PF00069	0.666
MOD_PKA_2	25	31	PF00069	0.714
MOD_PKA_2	322	328	PF00069	0.632
MOD_PKA_2	362	368	PF00069	0.476
MOD_PKA_2	507	513	PF00069	0.555
MOD_PKA_2	524	530	PF00069	0.710
MOD_PKA_2	539	545	PF00069	0.430
MOD_PKA_2	611	617	PF00069	0.622
MOD_PKA_2	647	653	PF00069	0.546
MOD_PKA_2	657	663	PF00069	0.644
MOD_PKA_2	672	678	PF00069	0.575
MOD_PKA_2	829	835	PF00069	0.487
MOD_PKA_2	861	867	PF00069	0.513
MOD_PKB_1	610	618	PF00069	0.496
MOD_Plk_1	231	237	PF00069	0.653
MOD_Plk_1	731	737	PF00069	0.427
MOD_Plk_1	78	84	PF00069	0.431
MOD_Plk_2-3	635	641	PF00069	0.487
MOD_Plk_4	237	243	PF00069	0.677
MOD_Plk_4	436	442	PF00069	0.384
MOD_Plk_4	46	52	PF00069	0.558
MOD_Plk_4	62	68	PF00069	0.479
MOD_Plk_4	731	737	PF00069	0.427
MOD_Plk_4	78	84	PF00069	0.335
MOD_Plk_4	881	887	PF00069	0.326
MOD_ProDKin_1	153	159	PF00069	0.714
MOD_ProDKin_1	171	177	PF00069	0.596
MOD_ProDKin_1	179	185	PF00069	0.609
MOD_ProDKin_1	19	25	PF00069	0.756
MOD_ProDKin_1	195	201	PF00069	0.700
MOD_ProDKin_1	221	227	PF00069	0.687
MOD_ProDKin_1	243	249	PF00069	0.696
MOD_ProDKin_1	324	330	PF00069	0.681
MOD_ProDKin_1	412	418	PF00069	0.528
MOD_ProDKin_1	509	515	PF00069	0.622
MOD_ProDKin_1	601	607	PF00069	0.618
MOD_ProDKin_1	696	702	PF00069	0.627
MOD_ProDKin_1	765	771	PF00069	0.638
MOD_SUMO_for_1	291	294	PF00179	0.503
MOD_SUMO_rev_2	531	539	PF00179	0.626
MOD_SUMO_rev_2	542	548	PF00179	0.449
TRG_DiLeu_BaEn_1	881	886	PF01217	0.476
TRG_DiLeu_BaLyEn_6	349	354	PF01217	0.428
TRG_DiLeu_BaLyEn_6	470	475	PF01217	0.391
TRG_DiLeu_BaLyEn_6	70	75	PF01217	0.351
TRG_ENDOCYTIC_2	308	311	PF00928	0.491
TRG_ENDOCYTIC_2	313	316	PF00928	0.418
TRG_ENDOCYTIC_2	551	554	PF00928	0.418
TRG_ENDOCYTIC_2	63	66	PF00928	0.406
TRG_ENDOCYTIC_2	794	797	PF00928	0.376
TRG_ER_diArg_1	10	13	PF00400	0.650
TRG_ER_diArg_1	147	150	PF00400	0.688
TRG_ER_diArg_1	249	251	PF00400	0.537
TRG_ER_diArg_1	72	74	PF00400	0.434
TRG_NLS_MonoExtN_4	249	256	PF00514	0.657
TRG_Pf-PMV_PEXEL_1	106	111	PF00026	0.496
TRG_Pf-PMV_PEXEL_1	165	170	PF00026	0.659
TRG_Pf-PMV_PEXEL_1	557	561	PF00026	0.392
TRG_Pf-PMV_PEXEL_1	72	77	PF00026	0.408

Homologs


Protein	Taxonomy	Sequence identity	Coverage
A0A0N1IIL4	Leptomonas seymouri	54%	100%
A0A3S7X053	Leishmania donovani	89%	100%
A4HF65	Leishmania braziliensis	77%	100%
A4I2E8	Leishmania infantum	90%	100%
C9ZX58	Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972)	33%	100%
Q4Q8X1	Leishmania major	88%	98%