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: 4 |
Pissara et al. | yes | yes: 20 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 10 |
GO:0043226 | organelle | 2 | 10 |
GO:0043227 | membrane-bounded organelle | 3 | 10 |
GO:0043229 | intracellular organelle | 3 | 10 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
GO:0000785 | chromatin | 2 | 1 |
Related structures:
AlphaFold database: E9ALJ0
Term | Name | Level | Count |
---|---|---|---|
GO:0006325 | chromatin organization | 4 | 10 |
GO:0006334 | nucleosome assembly | 7 | 10 |
GO:0006338 | chromatin remodeling | 5 | 10 |
GO:0009987 | cellular process | 1 | 10 |
GO:0016043 | cellular component organization | 3 | 10 |
GO:0022607 | cellular component assembly | 4 | 10 |
GO:0034728 | nucleosome organization | 6 | 10 |
GO:0043933 | protein-containing complex organization | 4 | 10 |
GO:0065003 | protein-containing complex assembly | 5 | 10 |
GO:0065004 | protein-DNA complex assembly | 6 | 10 |
GO:0071824 | protein-DNA complex subunit organization | 5 | 10 |
GO:0071840 | cellular component organization or biogenesis | 2 | 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003682 | chromatin binding | 2 | 1 |
GO:0005488 | binding | 1 | 1 |
GO:0005515 | protein binding | 2 | 1 |
GO:0042393 | histone binding | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 100 | 102 | PF00675 | 0.629 |
CLV_NRD_NRD_1 | 47 | 49 | PF00675 | 0.711 |
CLV_PCSK_KEX2_1 | 47 | 49 | PF00082 | 0.638 |
CLV_PCSK_SKI1_1 | 102 | 106 | PF00082 | 0.638 |
CLV_PCSK_SKI1_1 | 48 | 52 | PF00082 | 0.690 |
CLV_PCSK_SKI1_1 | 83 | 87 | PF00082 | 0.621 |
DEG_APCC_DBOX_1 | 47 | 55 | PF00400 | 0.700 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.653 |
DOC_CKS1_1 | 65 | 70 | PF01111 | 0.694 |
DOC_PP1_RVXF_1 | 99 | 106 | PF00149 | 0.715 |
DOC_USP7_UBL2_3 | 98 | 102 | PF12436 | 0.668 |
DOC_WW_Pin1_4 | 61 | 66 | PF00397 | 0.613 |
LIG_14-3-3_CanoR_1 | 142 | 151 | PF00244 | 0.661 |
LIG_14-3-3_CanoR_1 | 83 | 91 | PF00244 | 0.602 |
LIG_14-3-3_CanoR_1 | 93 | 100 | PF00244 | 0.628 |
LIG_APCC_ABBAyCdc20_2 | 108 | 114 | PF00400 | 0.600 |
LIG_CaM_IQ_9 | 85 | 100 | PF13499 | 0.676 |
LIG_EH_1 | 175 | 179 | PF12763 | 0.619 |
LIG_FHA_1 | 126 | 132 | PF00498 | 0.633 |
LIG_FHA_1 | 13 | 19 | PF00498 | 0.580 |
LIG_FHA_1 | 143 | 149 | PF00498 | 0.532 |
LIG_FHA_1 | 165 | 171 | PF00498 | 0.702 |
LIG_FHA_1 | 27 | 33 | PF00498 | 0.483 |
LIG_LIR_Apic_2 | 171 | 177 | PF02991 | 0.581 |
LIG_LIR_Gen_1 | 146 | 156 | PF02991 | 0.695 |
LIG_LIR_Gen_1 | 86 | 94 | PF02991 | 0.661 |
LIG_LIR_Nem_3 | 146 | 152 | PF02991 | 0.584 |
LIG_LIR_Nem_3 | 55 | 61 | PF02991 | 0.606 |
LIG_LIR_Nem_3 | 86 | 91 | PF02991 | 0.642 |
LIG_Pex14_2 | 152 | 156 | PF04695 | 0.658 |
LIG_SH2_CRK | 100 | 104 | PF00017 | 0.715 |
LIG_SH2_CRK | 174 | 178 | PF00017 | 0.672 |
LIG_SH2_GRB2like | 174 | 177 | PF00017 | 0.670 |
LIG_SH2_SRC | 174 | 177 | PF00017 | 0.693 |
LIG_SH3_3 | 62 | 68 | PF00018 | 0.634 |
LIG_WRC_WIRS_1 | 104 | 109 | PF05994 | 0.688 |
MOD_CK1_1 | 12 | 18 | PF00069 | 0.588 |
MOD_CK1_1 | 155 | 161 | PF00069 | 0.522 |
MOD_CK1_1 | 64 | 70 | PF00069 | 0.638 |
MOD_CK2_1 | 135 | 141 | PF00069 | 0.665 |
MOD_CK2_1 | 155 | 161 | PF00069 | 0.472 |
MOD_CK2_1 | 35 | 41 | PF00069 | 0.606 |
MOD_CK2_1 | 60 | 66 | PF00069 | 0.654 |
MOD_GlcNHglycan | 137 | 140 | PF01048 | 0.688 |
MOD_GlcNHglycan | 58 | 61 | PF01048 | 0.586 |
MOD_GlcNHglycan | 69 | 72 | PF01048 | 0.560 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.654 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.672 |
MOD_GSK3_1 | 52 | 59 | PF00069 | 0.659 |
MOD_GSK3_1 | 60 | 67 | PF00069 | 0.639 |
MOD_N-GLC_1 | 73 | 78 | PF02516 | 0.593 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.633 |
MOD_NEK2_1 | 126 | 131 | PF00069 | 0.690 |
MOD_NEK2_1 | 152 | 157 | PF00069 | 0.431 |
MOD_NEK2_1 | 50 | 55 | PF00069 | 0.499 |
MOD_NEK2_2 | 169 | 174 | PF00069 | 0.685 |
MOD_PIKK_1 | 1 | 7 | PF00454 | 0.598 |
MOD_PKA_2 | 92 | 98 | PF00069 | 0.628 |
MOD_PKB_1 | 142 | 150 | PF00069 | 0.660 |
MOD_Plk_1 | 27 | 33 | PF00069 | 0.667 |
MOD_Plk_2-3 | 17 | 23 | PF00069 | 0.601 |
MOD_Plk_4 | 144 | 150 | PF00069 | 0.583 |
MOD_Plk_4 | 169 | 175 | PF00069 | 0.684 |
MOD_ProDKin_1 | 61 | 67 | PF00069 | 0.613 |
MOD_SUMO_rev_2 | 119 | 129 | PF00179 | 0.680 |
MOD_SUMO_rev_2 | 95 | 99 | PF00179 | 0.656 |
TRG_DiLeu_BaEn_1 | 46 | 51 | PF01217 | 0.645 |
TRG_DiLeu_BaEn_4 | 27 | 33 | PF01217 | 0.706 |
TRG_DiLeu_BaLyEn_6 | 39 | 44 | PF01217 | 0.668 |
TRG_ENDOCYTIC_2 | 100 | 103 | PF00928 | 0.712 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I131 | Leptomonas seymouri | 75% | 100% |
A0A0S4JW42 | Bodo saltans | 37% | 92% |
A0A1X0P944 | Trypanosomatidae | 44% | 99% |
A0A3S7X2Q8 | Leishmania donovani | 93% | 100% |
A0A422MX53 | Trypanosoma rangeli | 46% | 99% |
A4HHN3 | Leishmania braziliensis | 81% | 100% |
A4I4U8 | Leishmania infantum | 93% | 100% |
C9ZLJ6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 100% |
E9AE96 | Leishmania major | 94% | 100% |
Q8LC68 | Arabidopsis thaliana | 25% | 72% |