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 |
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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: A4HCZ8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 11 | 15 | PF00656 | 0.738 |
CLV_C14_Caspase3-7 | 28 | 32 | PF00656 | 0.555 |
CLV_NRD_NRD_1 | 178 | 180 | PF00675 | 0.610 |
CLV_NRD_NRD_1 | 188 | 190 | PF00675 | 0.547 |
CLV_NRD_NRD_1 | 239 | 241 | PF00675 | 0.489 |
CLV_NRD_NRD_1 | 33 | 35 | PF00675 | 0.569 |
CLV_NRD_NRD_1 | 94 | 96 | PF00675 | 0.652 |
CLV_PCSK_KEX2_1 | 178 | 180 | PF00082 | 0.688 |
CLV_PCSK_KEX2_1 | 190 | 192 | PF00082 | 0.596 |
CLV_PCSK_KEX2_1 | 239 | 241 | PF00082 | 0.489 |
CLV_PCSK_KEX2_1 | 264 | 266 | PF00082 | 0.544 |
CLV_PCSK_KEX2_1 | 33 | 35 | PF00082 | 0.569 |
CLV_PCSK_KEX2_1 | 49 | 51 | PF00082 | 0.591 |
CLV_PCSK_KEX2_1 | 93 | 95 | PF00082 | 0.657 |
CLV_PCSK_PC1ET2_1 | 190 | 192 | PF00082 | 0.663 |
CLV_PCSK_PC1ET2_1 | 264 | 266 | PF00082 | 0.468 |
CLV_PCSK_PC1ET2_1 | 49 | 51 | PF00082 | 0.562 |
CLV_PCSK_PC7_1 | 260 | 266 | PF00082 | 0.489 |
CLV_PCSK_SKI1_1 | 158 | 162 | PF00082 | 0.607 |
CLV_PCSK_SKI1_1 | 178 | 182 | PF00082 | 0.397 |
CLV_PCSK_SKI1_1 | 191 | 195 | PF00082 | 0.575 |
CLV_PCSK_SKI1_1 | 34 | 38 | PF00082 | 0.570 |
CLV_PCSK_SKI1_1 | 50 | 54 | PF00082 | 0.706 |
CLV_PCSK_SKI1_1 | 97 | 101 | PF00082 | 0.756 |
DEG_SPOP_SBC_1 | 16 | 20 | PF00917 | 0.778 |
DOC_CYCLIN_RxL_1 | 152 | 164 | PF00134 | 0.709 |
DOC_CYCLIN_RxL_1 | 93 | 105 | PF00134 | 0.647 |
DOC_CYCLIN_yCln2_LP_2 | 53 | 56 | PF00134 | 0.550 |
DOC_MAPK_gen_1 | 93 | 101 | PF00069 | 0.622 |
DOC_PP2B_LxvP_1 | 213 | 216 | PF13499 | 0.528 |
DOC_PP2B_LxvP_1 | 53 | 56 | PF13499 | 0.550 |
DOC_USP7_MATH_1 | 119 | 123 | PF00917 | 0.476 |
DOC_USP7_MATH_1 | 148 | 152 | PF00917 | 0.741 |
DOC_USP7_MATH_1 | 17 | 21 | PF00917 | 0.781 |
DOC_USP7_MATH_1 | 195 | 199 | PF00917 | 0.629 |
DOC_USP7_MATH_1 | 43 | 47 | PF00917 | 0.693 |
DOC_USP7_MATH_1 | 56 | 60 | PF00917 | 0.747 |
DOC_USP7_MATH_1 | 8 | 12 | PF00917 | 0.733 |
DOC_USP7_MATH_2 | 27 | 33 | PF00917 | 0.555 |
DOC_WW_Pin1_4 | 23 | 28 | PF00397 | 0.584 |
DOC_WW_Pin1_4 | 79 | 84 | PF00397 | 0.594 |
LIG_14-3-3_CanoR_1 | 158 | 163 | PF00244 | 0.607 |
LIG_14-3-3_CanoR_1 | 94 | 100 | PF00244 | 0.601 |
LIG_BRCT_BRCA1_1 | 103 | 107 | PF00533 | 0.738 |
LIG_FHA_1 | 140 | 146 | PF00498 | 0.616 |
LIG_FHA_1 | 96 | 102 | PF00498 | 0.627 |
LIG_FHA_2 | 112 | 118 | PF00498 | 0.557 |
LIG_FHA_2 | 159 | 165 | PF00498 | 0.599 |
LIG_FHA_2 | 224 | 230 | PF00498 | 0.600 |
LIG_FHA_2 | 85 | 91 | PF00498 | 0.647 |
LIG_Integrin_RGD_1 | 12 | 14 | PF01839 | 0.557 |
LIG_PCNA_yPIPBox_3 | 124 | 136 | PF02747 | 0.452 |
LIG_Pex14_2 | 107 | 111 | PF04695 | 0.635 |
LIG_SH2_SRC | 221 | 224 | PF00017 | 0.492 |
LIG_SH2_STAP1 | 168 | 172 | PF00017 | 0.682 |
LIG_SH2_STAP1 | 241 | 245 | PF00017 | 0.645 |
LIG_SH3_3 | 49 | 55 | PF00018 | 0.557 |
LIG_SUMO_SIM_par_1 | 134 | 143 | PF11976 | 0.435 |
LIG_SUMO_SIM_par_1 | 158 | 164 | PF11976 | 0.704 |
LIG_TRAF2_1 | 161 | 164 | PF00917 | 0.583 |
MOD_CDK_SPxK_1 | 79 | 85 | PF00069 | 0.559 |
MOD_CK1_1 | 15 | 21 | PF00069 | 0.735 |
MOD_CK1_1 | 151 | 157 | PF00069 | 0.741 |
MOD_CK1_1 | 208 | 214 | PF00069 | 0.763 |
MOD_CK1_1 | 22 | 28 | PF00069 | 0.661 |
MOD_CK1_1 | 59 | 65 | PF00069 | 0.569 |
MOD_CK1_1 | 76 | 82 | PF00069 | 0.617 |
MOD_CK1_1 | 84 | 90 | PF00069 | 0.698 |
MOD_CK2_1 | 111 | 117 | PF00069 | 0.616 |
MOD_CK2_1 | 158 | 164 | PF00069 | 0.604 |
MOD_CK2_1 | 223 | 229 | PF00069 | 0.618 |
MOD_CK2_1 | 23 | 29 | PF00069 | 0.691 |
MOD_CK2_1 | 84 | 90 | PF00069 | 0.656 |
MOD_GlcNHglycan | 148 | 151 | PF01048 | 0.591 |
MOD_GlcNHglycan | 197 | 200 | PF01048 | 0.731 |
MOD_GlcNHglycan | 21 | 24 | PF01048 | 0.730 |
MOD_GlcNHglycan | 210 | 213 | PF01048 | 0.731 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.675 |
MOD_GSK3_1 | 191 | 198 | PF00069 | 0.711 |
MOD_GSK3_1 | 62 | 69 | PF00069 | 0.816 |
MOD_GSK3_1 | 75 | 82 | PF00069 | 0.705 |
MOD_GSK3_1 | 8 | 15 | PF00069 | 0.725 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.627 |
MOD_NEK2_1 | 111 | 116 | PF00069 | 0.461 |
MOD_NEK2_1 | 138 | 143 | PF00069 | 0.670 |
MOD_NEK2_1 | 146 | 151 | PF00069 | 0.403 |
MOD_NEK2_1 | 258 | 263 | PF00069 | 0.549 |
MOD_NEK2_2 | 119 | 124 | PF00069 | 0.476 |
MOD_PK_1 | 12 | 18 | PF00069 | 0.779 |
MOD_PKB_1 | 189 | 197 | PF00069 | 0.748 |
MOD_PKB_1 | 93 | 101 | PF00069 | 0.516 |
MOD_Plk_1 | 119 | 125 | PF00069 | 0.529 |
MOD_Plk_2-3 | 223 | 229 | PF00069 | 0.451 |
MOD_Plk_4 | 95 | 101 | PF00069 | 0.621 |
MOD_ProDKin_1 | 23 | 29 | PF00069 | 0.585 |
MOD_ProDKin_1 | 79 | 85 | PF00069 | 0.594 |
TRG_DiLeu_BaLyEn_6 | 141 | 146 | PF01217 | 0.445 |
TRG_ER_diArg_1 | 177 | 179 | PF00400 | 0.718 |
TRG_ER_diArg_1 | 188 | 191 | PF00400 | 0.579 |
TRG_ER_diArg_1 | 238 | 240 | PF00400 | 0.479 |
TRG_ER_diArg_1 | 93 | 95 | PF00400 | 0.595 |
TRG_NLS_Bipartite_1 | 178 | 193 | PF00514 | 0.703 |
TRG_Pf-PMV_PEXEL_1 | 158 | 163 | PF00026 | 0.597 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4W9 | Leptomonas seymouri | 49% | 100% |
A0A3S7WXU2 | Leishmania donovani | 71% | 100% |
A4I0I3 | Leishmania infantum | 70% | 100% |
E9AWE5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 67% | 100% |
Q4QB27 | Leishmania major | 70% | 100% |