FHA domain-containing protein

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

Quick info

Protein:

Gene product:

hypothetical protein, conserved

Species:

Leishmania major

UniProt:

Q4QEF3_LEIMA

TriTrypDb:

LmjF.17.0410 , LMJLV39_170009800 , LMJSD75_170009500

Length:

1062

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: 8
NetGPI	no	yes: 0, no: 8

Cellular components
Term	Name	Level	Count
GO:0030870	Mre11 complex	3	2
GO:0032991	protein-containing complex	1	2
GO:0140513	nuclear protein-containing complex	2	2

Expansion

Sequence features

Q4QEF3

Sequence

MSA

Disorder

Secondary

Topology

Domains

SignalP

GPI

Phosphorylations

ELMs

Structure

Predicted structure by AlphaFold2

Related structures:

AlphaFold database: Q4QEF3

Function

Biological processes
Term	Name	Level	Count
GO:0000075	cell cycle checkpoint signaling	4	2
GO:0000077	DNA damage checkpoint signaling	5	2
GO:0006139	nucleobase-containing compound metabolic process	3	2
GO:0006259	DNA metabolic process	4	2
GO:0006281	DNA repair	5	2
GO:0006302	double-strand break repair	6	2
GO:0006725	cellular aromatic compound metabolic process	3	2
GO:0006807	nitrogen compound metabolic process	2	2
GO:0006950	response to stress	2	2
GO:0006974	DNA damage response	4	2
GO:0007093	mitotic cell cycle checkpoint signaling	4	2
GO:0007095	mitotic G2 DNA damage checkpoint signaling	6	2
GO:0007165	signal transduction	2	2
GO:0007346	regulation of mitotic cell cycle	5	2
GO:0008152	metabolic process	1	2
GO:0009987	cellular process	1	2
GO:0010389	regulation of G2/M transition of mitotic cell cycle	7	2
GO:0010564	regulation of cell cycle process	5	2
GO:0010948	negative regulation of cell cycle process	6	2
GO:0010972	negative regulation of G2/M transition of mitotic cell cycle	8	2
GO:0022402	cell cycle process	2	2
GO:0031570	DNA integrity checkpoint signaling	5	2
GO:0033554	cellular response to stress	3	2
GO:0034641	cellular nitrogen compound metabolic process	3	2
GO:0035556	intracellular signal transduction	3	2
GO:0042770	signal transduction in response to DNA damage	4	2
GO:0043170	macromolecule metabolic process	3	2
GO:0044237	cellular metabolic process	2	2
GO:0044238	primary metabolic process	2	2
GO:0044260	obsolete cellular macromolecule metabolic process	3	2
GO:0044773	mitotic DNA damage checkpoint signaling	6	2
GO:0044774	mitotic DNA integrity checkpoint signaling	5	2
GO:0044818	mitotic G2/M transition checkpoint	5	2
GO:0045786	negative regulation of cell cycle	5	2
GO:0045930	negative regulation of mitotic cell cycle	6	2
GO:0046483	heterocycle metabolic process	3	2
GO:0048519	negative regulation of biological process	3	2
GO:0048523	negative regulation of cellular process	4	2
GO:0050789	regulation of biological process	2	2
GO:0050794	regulation of cellular process	3	2
GO:0050896	response to stimulus	1	2
GO:0051716	cellular response to stimulus	2	2
GO:0051726	regulation of cell cycle	4	2
GO:0065007	biological regulation	1	2
GO:0071704	organic substance metabolic process	2	2
GO:0090304	nucleic acid metabolic process	4	2
GO:1901360	organic cyclic compound metabolic process	3	2
GO:1901987	regulation of cell cycle phase transition	6	2
GO:1901988	negative regulation of cell cycle phase transition	7	2
GO:1901990	regulation of mitotic cell cycle phase transition	6	2
GO:1901991	negative regulation of mitotic cell cycle phase transition	7	2
GO:1902749	regulation of cell cycle G2/M phase transition	7	2
GO:1902750	negative regulation of cell cycle G2/M phase transition	8	2
GO:1903047	mitotic cell cycle process	3	2

Could not find GO molecular_function term for this entry.

Putative motif mimicry


Leishmania	From	To	Domain/Motif	Score
CLV_C14_Caspase3-7	114	118	PF00656	0.467
CLV_C14_Caspase3-7	207	211	PF00656	0.427
CLV_C14_Caspase3-7	673	677	PF00656	0.665
CLV_C14_Caspase3-7	711	715	PF00656	0.634
CLV_C14_Caspase3-7	785	789	PF00656	0.548
CLV_C14_Caspase3-7	961	965	PF00656	0.629
CLV_NRD_NRD_1	1016	1018	PF00675	0.739
CLV_NRD_NRD_1	22	24	PF00675	0.417
CLV_NRD_NRD_1	493	495	PF00675	0.640
CLV_NRD_NRD_1	545	547	PF00675	0.575
CLV_NRD_NRD_1	665	667	PF00675	0.581
CLV_NRD_NRD_1	670	672	PF00675	0.646
CLV_NRD_NRD_1	678	680	PF00675	0.622
CLV_NRD_NRD_1	801	803	PF00675	0.714
CLV_NRD_NRD_1	858	860	PF00675	0.792
CLV_NRD_NRD_1	901	903	PF00675	0.685
CLV_NRD_NRD_1	990	992	PF00675	0.706
CLV_PCSK_KEX2_1	1007	1009	PF00082	0.542
CLV_PCSK_KEX2_1	1016	1018	PF00082	0.629
CLV_PCSK_KEX2_1	493	495	PF00082	0.717
CLV_PCSK_KEX2_1	544	546	PF00082	0.584
CLV_PCSK_KEX2_1	665	667	PF00082	0.586
CLV_PCSK_KEX2_1	670	672	PF00082	0.646
CLV_PCSK_KEX2_1	678	680	PF00082	0.622
CLV_PCSK_KEX2_1	801	803	PF00082	0.718
CLV_PCSK_KEX2_1	901	903	PF00082	0.685
CLV_PCSK_KEX2_1	990	992	PF00082	0.756
CLV_PCSK_PC1ET2_1	1007	1009	PF00082	0.679
CLV_PCSK_PC7_1	489	495	PF00082	0.597
CLV_PCSK_PC7_1	666	672	PF00082	0.629
CLV_PCSK_PC7_1	797	803	PF00082	0.692
CLV_PCSK_SKI1_1	301	305	PF00082	0.326
CLV_PCSK_SKI1_1	583	587	PF00082	0.414
CLV_PCSK_SKI1_1	665	669	PF00082	0.569
CLV_PCSK_SKI1_1	678	682	PF00082	0.684
CLV_PCSK_SKI1_1	684	688	PF00082	0.671
DEG_APCC_DBOX_1	876	884	PF00400	0.691
DEG_COP1_1	960	971	PF00400	0.627
DEG_Nend_Nbox_1	1	3	PF02207	0.336
DEG_SPOP_SBC_1	264	268	PF00917	0.581
DEG_SPOP_SBC_1	462	466	PF00917	0.635
DEG_SPOP_SBC_1	789	793	PF00917	0.560
DEG_SPOP_SBC_1	942	946	PF00917	0.635
DOC_MAPK_gen_1	544	550	PF00069	0.547
DOC_MAPK_gen_1	801	807	PF00069	0.548
DOC_MAPK_MEF2A_6	152	160	PF00069	0.328
DOC_PP1_RVXF_1	299	305	PF00149	0.421
DOC_PP2B_LxvP_1	248	251	PF13499	0.417
DOC_PP2B_LxvP_1	876	879	PF13499	0.764
DOC_PP4_FxxP_1	254	257	PF00568	0.388
DOC_PP4_FxxP_1	282	285	PF00568	0.576
DOC_SPAK_OSR1_1	253	257	PF12202	0.454
DOC_USP7_MATH_1	11	15	PF00917	0.438
DOC_USP7_MATH_1	188	192	PF00917	0.450
DOC_USP7_MATH_1	249	253	PF00917	0.584
DOC_USP7_MATH_1	283	287	PF00917	0.545
DOC_USP7_MATH_1	403	407	PF00917	0.328
DOC_USP7_MATH_1	447	451	PF00917	0.766
DOC_USP7_MATH_1	479	483	PF00917	0.596
DOC_USP7_MATH_1	522	526	PF00917	0.756
DOC_USP7_MATH_1	527	531	PF00917	0.633
DOC_USP7_MATH_1	638	642	PF00917	0.555
DOC_USP7_MATH_1	680	684	PF00917	0.627
DOC_USP7_MATH_1	707	711	PF00917	0.702
DOC_USP7_MATH_1	731	735	PF00917	0.735
DOC_USP7_MATH_1	747	751	PF00917	0.589
DOC_USP7_MATH_1	790	794	PF00917	0.605
DOC_USP7_MATH_1	796	800	PF00917	0.584
DOC_USP7_MATH_1	830	834	PF00917	0.630
DOC_USP7_MATH_1	986	990	PF00917	0.715
DOC_USP7_MATH_2	752	758	PF00917	0.631
DOC_WW_Pin1_4	1011	1016	PF00397	0.701
DOC_WW_Pin1_4	377	382	PF00397	0.512
DOC_WW_Pin1_4	518	523	PF00397	0.762
DOC_WW_Pin1_4	694	699	PF00397	0.626
DOC_WW_Pin1_4	7	12	PF00397	0.500
DOC_WW_Pin1_4	779	784	PF00397	0.688
DOC_WW_Pin1_4	862	867	PF00397	0.719
DOC_WW_Pin1_4	888	893	PF00397	0.696
DOC_WW_Pin1_4	946	951	PF00397	0.613
LIG_14-3-3_CanoR_1	259	264	PF00244	0.428
LIG_14-3-3_CanoR_1	483	490	PF00244	0.716
LIG_14-3-3_CanoR_1	493	499	PF00244	0.666
LIG_14-3-3_CanoR_1	569	574	PF00244	0.350
LIG_14-3-3_CanoR_1	656	663	PF00244	0.505
LIG_14-3-3_CanoR_1	678	686	PF00244	0.642
LIG_14-3-3_CanoR_1	797	805	PF00244	0.709
LIG_14-3-3_CanoR_1	859	868	PF00244	0.699
LIG_14-3-3_CanoR_1	985	992	PF00244	0.757
LIG_14-3-3_CanoR_1	999	1004	PF00244	0.621
LIG_APCC_ABBA_1	451	456	PF00400	0.765
LIG_APCC_ABBAyCdc20_2	294	300	PF00400	0.289
LIG_BRCT_BRCA1_1	412	416	PF00533	0.439
LIG_DLG_GKlike_1	494	502	PF00625	0.512
LIG_DLG_GKlike_1	801	808	PF00625	0.546
LIG_FHA_1	265	271	PF00498	0.523
LIG_FHA_1	407	413	PF00498	0.424
LIG_FHA_1	570	576	PF00498	0.353
LIG_FHA_1	628	634	PF00498	0.444
LIG_FHA_1	662	668	PF00498	0.685
LIG_FHA_1	938	944	PF00498	0.660
LIG_FHA_2	112	118	PF00498	0.452
LIG_FHA_2	181	187	PF00498	0.445
LIG_FHA_2	643	649	PF00498	0.364
LIG_FHA_2	783	789	PF00498	0.542
LIG_FHA_2	919	925	PF00498	0.735
LIG_FHA_2	929	935	PF00498	0.721
LIG_LIR_Apic_2	252	257	PF02991	0.477
LIG_LIR_Apic_2	266	272	PF02991	0.423
LIG_LIR_Apic_2	280	285	PF02991	0.494
LIG_LIR_Gen_1	219	230	PF02991	0.331
LIG_LIR_Gen_1	232	242	PF02991	0.321
LIG_LIR_Gen_1	276	285	PF02991	0.535
LIG_LIR_Gen_1	357	364	PF02991	0.424
LIG_LIR_Gen_1	406	416	PF02991	0.353
LIG_LIR_Gen_1	561	571	PF02991	0.390
LIG_LIR_Nem_3	14	20	PF02991	0.367
LIG_LIR_Nem_3	150	156	PF02991	0.420
LIG_LIR_Nem_3	219	225	PF02991	0.330
LIG_LIR_Nem_3	228	234	PF02991	0.300
LIG_LIR_Nem_3	276	282	PF02991	0.511
LIG_LIR_Nem_3	300	306	PF02991	0.349
LIG_LIR_Nem_3	357	363	PF02991	0.426
LIG_LIR_Nem_3	37	43	PF02991	0.384
LIG_LIR_Nem_3	406	411	PF02991	0.364
LIG_LIR_Nem_3	561	566	PF02991	0.388
LIG_LIR_Nem_3	870	876	PF02991	0.635
LIG_LYPXL_yS_3	873	876	PF13949	0.644
LIG_Pex14_2	559	563	PF04695	0.452
LIG_PTAP_UEV_1	968	973	PF05743	0.647
LIG_PTB_Apo_2	411	418	PF02174	0.451
LIG_PTB_Phospho_1	411	417	PF10480	0.443
LIG_RPA_C_Fungi	478	490	PF08784	0.593
LIG_SH2_CRK	153	157	PF00017	0.421
LIG_SH2_CRK	18	22	PF00017	0.353
LIG_SH2_CRK	222	226	PF00017	0.310
LIG_SH2_CRK	571	575	PF00017	0.449
LIG_SH2_GRB2like	169	172	PF00017	0.430
LIG_SH2_NCK_1	222	226	PF00017	0.310
LIG_SH2_PTP2	360	363	PF00017	0.326
LIG_SH2_SRC	360	363	PF00017	0.420
LIG_SH2_SRC	417	420	PF00017	0.510
LIG_SH2_STAP1	18	22	PF00017	0.288
LIG_SH2_STAP1	2	6	PF00017	0.484
LIG_SH2_STAP1	571	575	PF00017	0.465
LIG_SH2_STAP1	601	605	PF00017	0.424
LIG_SH2_STAP1	629	633	PF00017	0.432
LIG_SH2_STAT5	142	145	PF00017	0.437
LIG_SH2_STAT5	203	206	PF00017	0.357
LIG_SH2_STAT5	229	232	PF00017	0.324
LIG_SH2_STAT5	26	29	PF00017	0.318
LIG_SH2_STAT5	269	272	PF00017	0.381
LIG_SH2_STAT5	360	363	PF00017	0.326
LIG_SH2_STAT5	562	565	PF00017	0.392
LIG_SH2_STAT5	571	574	PF00017	0.300
LIG_SH2_STAT5	592	595	PF00017	0.483
LIG_SH2_STAT5	629	632	PF00017	0.457
LIG_SH3_2	872	877	PF14604	0.645
LIG_SH3_2	992	997	PF14604	0.559
LIG_SH3_3	182	188	PF00018	0.405
LIG_SH3_3	192	198	PF00018	0.419
LIG_SH3_3	322	328	PF00018	0.443
LIG_SH3_3	784	790	PF00018	0.619
LIG_SH3_3	855	861	PF00018	0.587
LIG_SH3_3	868	874	PF00018	0.626
LIG_SH3_3	891	897	PF00018	0.673
LIG_SH3_3	966	972	PF00018	0.627
LIG_SH3_3	989	995	PF00018	0.710
LIG_SH3_4	848	855	PF00018	0.561
LIG_SUMO_SIM_anti_2	49	55	PF11976	0.334
LIG_TRAF2_1	83	86	PF00917	0.774
LIG_TRAF2_1	913	916	PF00917	0.767
LIG_TRFH_1	279	283	PF08558	0.467
LIG_TYR_ITIM	38	43	PF00017	0.472
LIG_TYR_ITIM	560	565	PF00017	0.392
LIG_TYR_ITIM	871	876	PF00017	0.620
LIG_UBA3_1	407	415	PF00899	0.437
LIG_WRC_WIRS_1	570	575	PF05994	0.301
MOD_CDC14_SPxK_1	10	13	PF00782	0.519
MOD_CDK_SPK_2	1011	1016	PF00069	0.588
MOD_CDK_SPxK_1	1011	1017	PF00069	0.751
MOD_CDK_SPxK_1	7	13	PF00069	0.505
MOD_CK1_1	1011	1017	PF00069	0.772
MOD_CK1_1	129	135	PF00069	0.333
MOD_CK1_1	394	400	PF00069	0.544
MOD_CK1_1	406	412	PF00069	0.375
MOD_CK1_1	488	494	PF00069	0.686
MOD_CK1_1	674	680	PF00069	0.649
MOD_CK1_1	682	688	PF00069	0.610
MOD_CK1_1	7	13	PF00069	0.505
MOD_CK1_1	782	788	PF00069	0.762
MOD_CK1_1	791	797	PF00069	0.737
MOD_CK1_1	803	809	PF00069	0.722
MOD_CK1_1	89	95	PF00069	0.545
MOD_CK1_1	927	933	PF00069	0.585
MOD_CK2_1	249	255	PF00069	0.505
MOD_CK2_1	341	347	PF00069	0.533
MOD_CK2_1	371	377	PF00069	0.460
MOD_CK2_1	625	631	PF00069	0.563
MOD_CK2_1	642	648	PF00069	0.350
MOD_CK2_1	733	739	PF00069	0.590
MOD_CK2_1	910	916	PF00069	0.701
MOD_CK2_1	918	924	PF00069	0.744
MOD_CK2_1	928	934	PF00069	0.714
MOD_CK2_1	946	952	PF00069	0.554
MOD_Cter_Amidation	542	545	PF01082	0.592
MOD_GlcNHglycan	1003	1006	PF01048	0.669
MOD_GlcNHglycan	1010	1013	PF01048	0.621
MOD_GlcNHglycan	1038	1042	PF01048	0.806
MOD_GlcNHglycan	128	131	PF01048	0.638
MOD_GlcNHglycan	13	16	PF01048	0.443
MOD_GlcNHglycan	161	165	PF01048	0.424
MOD_GlcNHglycan	308	312	PF01048	0.349
MOD_GlcNHglycan	373	376	PF01048	0.488
MOD_GlcNHglycan	393	396	PF01048	0.259
MOD_GlcNHglycan	444	448	PF01048	0.810
MOD_GlcNHglycan	465	468	PF01048	0.634
MOD_GlcNHglycan	471	474	PF01048	0.660
MOD_GlcNHglycan	475	478	PF01048	0.686
MOD_GlcNHglycan	485	488	PF01048	0.610
MOD_GlcNHglycan	522	525	PF01048	0.682
MOD_GlcNHglycan	538	541	PF01048	0.572
MOD_GlcNHglycan	658	661	PF01048	0.540
MOD_GlcNHglycan	735	738	PF01048	0.812
MOD_GlcNHglycan	775	778	PF01048	0.756
MOD_GlcNHglycan	794	797	PF01048	0.695
MOD_GlcNHglycan	812	815	PF01048	0.651
MOD_GlcNHglycan	88	91	PF01048	0.748
MOD_GlcNHglycan	898	901	PF01048	0.700
MOD_GlcNHglycan	904	907	PF01048	0.669
MOD_GlcNHglycan	969	972	PF01048	0.664
MOD_GlcNHglycan	979	982	PF01048	0.719
MOD_GlcNHglycan	992	995	PF01048	0.715
MOD_GSK3_1	107	114	PF00069	0.448
MOD_GSK3_1	122	129	PF00069	0.498
MOD_GSK3_1	216	223	PF00069	0.537
MOD_GSK3_1	258	265	PF00069	0.553
MOD_GSK3_1	273	280	PF00069	0.379
MOD_GSK3_1	283	290	PF00069	0.427
MOD_GSK3_1	390	397	PF00069	0.540
MOD_GSK3_1	406	413	PF00069	0.265
MOD_GSK3_1	433	440	PF00069	0.625
MOD_GSK3_1	443	450	PF00069	0.785
MOD_GSK3_1	469	476	PF00069	0.745
MOD_GSK3_1	479	486	PF00069	0.599
MOD_GSK3_1	502	509	PF00069	0.543
MOD_GSK3_1	518	525	PF00069	0.713
MOD_GSK3_1	625	632	PF00069	0.469
MOD_GSK3_1	638	645	PF00069	0.376
MOD_GSK3_1	666	673	PF00069	0.727
MOD_GSK3_1	674	681	PF00069	0.703
MOD_GSK3_1	7	14	PF00069	0.499
MOD_GSK3_1	788	795	PF00069	0.700
MOD_GSK3_1	796	803	PF00069	0.617
MOD_GSK3_1	806	813	PF00069	0.518
MOD_GSK3_1	862	869	PF00069	0.770
MOD_GSK3_1	924	931	PF00069	0.613
MOD_GSK3_1	933	940	PF00069	0.622
MOD_GSK3_1	942	949	PF00069	0.658
MOD_GSK3_1	963	970	PF00069	0.645
MOD_GSK3_1	977	984	PF00069	0.634
MOD_GSK3_1	986	993	PF00069	0.664
MOD_GSK3_1	999	1006	PF00069	0.579
MOD_LATS_1	1035	1041	PF00433	0.650
MOD_N-GLC_1	1008	1013	PF02516	0.671
MOD_N-GLC_1	208	213	PF02516	0.401
MOD_N-GLC_1	290	295	PF02516	0.502
MOD_N-GLC_1	364	369	PF02516	0.437
MOD_N-GLC_1	731	736	PF02516	0.628
MOD_N-GLC_1	838	843	PF02516	0.703
MOD_N-GLC_1	957	962	PF02516	0.647
MOD_N-GLC_1	999	1004	PF02516	0.781
MOD_N-GLC_2	623	625	PF02516	0.443
MOD_NEK2_1	122	127	PF00069	0.431
MOD_NEK2_1	160	165	PF00069	0.347
MOD_NEK2_1	180	185	PF00069	0.305
MOD_NEK2_1	208	213	PF00069	0.430
MOD_NEK2_1	341	346	PF00069	0.479
MOD_NEK2_1	371	376	PF00069	0.475
MOD_NEK2_1	4	9	PF00069	0.482
MOD_NEK2_1	506	511	PF00069	0.498
MOD_NEK2_1	536	541	PF00069	0.690
MOD_NEK2_1	773	778	PF00069	0.582
MOD_NEK2_1	808	813	PF00069	0.808
MOD_NEK2_1	943	948	PF00069	0.718
MOD_NEK2_2	403	408	PF00069	0.340
MOD_NEK2_2	629	634	PF00069	0.437
MOD_PIKK_1	1048	1054	PF00454	0.661
MOD_PIKK_1	341	347	PF00454	0.487
MOD_PIKK_1	506	512	PF00454	0.486
MOD_PIKK_1	747	753	PF00454	0.778
MOD_PIKK_1	838	844	PF00454	0.610
MOD_PIKK_1	910	916	PF00454	0.686
MOD_PIKK_1	944	950	PF00454	0.828
MOD_PIKK_1	963	969	PF00454	0.546
MOD_PK_1	1055	1061	PF00069	0.543
MOD_PK_1	819	825	PF00069	0.616
MOD_PK_1	999	1005	PF00069	0.564
MOD_PKA_1	493	499	PF00069	0.614
MOD_PKA_1	670	676	PF00069	0.667
MOD_PKA_1	678	684	PF00069	0.605
MOD_PKA_1	801	807	PF00069	0.678
MOD_PKA_1	990	996	PF00069	0.681
MOD_PKA_2	107	113	PF00069	0.443
MOD_PKA_2	258	264	PF00069	0.524
MOD_PKA_2	488	494	PF00069	0.702
MOD_PKA_2	595	601	PF00069	0.404
MOD_PKA_2	670	676	PF00069	0.718
MOD_PKA_2	678	684	PF00069	0.666
MOD_PKA_2	796	802	PF00069	0.710
MOD_PKA_2	977	983	PF00069	0.777
MOD_PKA_2	984	990	PF00069	0.795
MOD_PKB_1	483	491	PF00069	0.643
MOD_PKB_1	567	575	PF00069	0.310
MOD_Plk_1	1037	1043	PF00069	0.652
MOD_Plk_1	123	129	PF00069	0.438
MOD_Plk_1	160	166	PF00069	0.351
MOD_Plk_1	307	313	PF00069	0.275
MOD_Plk_1	34	40	PF00069	0.361
MOD_Plk_1	403	409	PF00069	0.344
MOD_Plk_1	443	449	PF00069	0.531
MOD_Plk_1	654	660	PF00069	0.508
MOD_Plk_1	963	969	PF00069	0.694
MOD_Plk_1	999	1005	PF00069	0.682
MOD_Plk_2-3	41	47	PF00069	0.379
MOD_Plk_2-3	595	601	PF00069	0.496
MOD_Plk_4	1055	1061	PF00069	0.556
MOD_Plk_4	16	22	PF00069	0.405
MOD_Plk_4	180	186	PF00069	0.398
MOD_Plk_4	220	226	PF00069	0.319
MOD_Plk_4	265	271	PF00069	0.652
MOD_Plk_4	403	409	PF00069	0.388
MOD_Plk_4	48	54	PF00069	0.348
MOD_Plk_4	569	575	PF00069	0.348
MOD_Plk_4	803	809	PF00069	0.544
MOD_Plk_4	890	896	PF00069	0.636
MOD_ProDKin_1	1011	1017	PF00069	0.704
MOD_ProDKin_1	377	383	PF00069	0.502
MOD_ProDKin_1	518	524	PF00069	0.764
MOD_ProDKin_1	694	700	PF00069	0.629
MOD_ProDKin_1	7	13	PF00069	0.505
MOD_ProDKin_1	779	785	PF00069	0.692
MOD_ProDKin_1	862	868	PF00069	0.719
MOD_ProDKin_1	888	894	PF00069	0.697
MOD_ProDKin_1	946	952	PF00069	0.617
MOD_SUMO_rev_2	577	581	PF00179	0.442
MOD_SUMO_rev_2	600	607	PF00179	0.384
TRG_DiLeu_BaEn_1	101	106	PF01217	0.397
TRG_DiLeu_BaEn_2	381	387	PF01217	0.467
TRG_DiLeu_BaEn_2	554	560	PF01217	0.487
TRG_DiLeu_BaEn_4	418	424	PF01217	0.538
TRG_ENDOCYTIC_2	153	156	PF00928	0.423
TRG_ENDOCYTIC_2	17	20	PF00928	0.338
TRG_ENDOCYTIC_2	222	225	PF00928	0.301
TRG_ENDOCYTIC_2	360	363	PF00928	0.326
TRG_ENDOCYTIC_2	40	43	PF00928	0.479
TRG_ENDOCYTIC_2	562	565	PF00928	0.380
TRG_ENDOCYTIC_2	571	574	PF00928	0.438
TRG_ENDOCYTIC_2	873	876	PF00928	0.655
TRG_ER_diArg_1	1015	1017	PF00400	0.719
TRG_ER_diArg_1	511	514	PF00400	0.543
TRG_ER_diArg_1	544	546	PF00400	0.666
TRG_ER_diArg_1	566	569	PF00400	0.357
TRG_ER_diArg_1	665	667	PF00400	0.562
TRG_ER_diArg_1	895	898	PF00400	0.699
TRG_ER_diArg_1	990	992	PF00400	0.738
TRG_NES_CRM1_1	179	193	PF08389	0.369
TRG_NES_CRM1_1	564	578	PF08389	0.387

Homologs


Protein	Taxonomy	Sequence identity	Coverage
A0A0N1I2V4	Leptomonas seymouri	48%	97%
A0A3S5H703	Leishmania donovani	87%	100%
A0A3S5IS81	Trypanosoma rangeli	32%	100%
A4H8Y4	Leishmania braziliensis	56%	92%
A4HXB4	Leishmania infantum	84%	100%
E9AR10	Leishmania mexicana (strain MHOM/GT/2001/U1103)	81%	99%
V5D6I4	Trypanosoma cruzi	30%	100%