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: 5 |
NetGPI | no | yes: 0, no: 5 |
Related structures:
AlphaFold database: Q4QCT9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 113 | 115 | PF00675 | 0.560 |
CLV_NRD_NRD_1 | 160 | 162 | PF00675 | 0.679 |
CLV_NRD_NRD_1 | 183 | 185 | PF00675 | 0.580 |
CLV_NRD_NRD_1 | 198 | 200 | PF00675 | 0.593 |
CLV_NRD_NRD_1 | 207 | 209 | PF00675 | 0.762 |
CLV_NRD_NRD_1 | 221 | 223 | PF00675 | 0.626 |
CLV_NRD_NRD_1 | 226 | 228 | PF00675 | 0.579 |
CLV_NRD_NRD_1 | 248 | 250 | PF00675 | 0.622 |
CLV_NRD_NRD_1 | 287 | 289 | PF00675 | 0.730 |
CLV_NRD_NRD_1 | 83 | 85 | PF00675 | 0.539 |
CLV_NRD_NRD_1 | 97 | 99 | PF00675 | 0.515 |
CLV_PCSK_KEX2_1 | 113 | 115 | PF00082 | 0.560 |
CLV_PCSK_KEX2_1 | 158 | 160 | PF00082 | 0.696 |
CLV_PCSK_KEX2_1 | 182 | 184 | PF00082 | 0.591 |
CLV_PCSK_KEX2_1 | 207 | 209 | PF00082 | 0.787 |
CLV_PCSK_KEX2_1 | 225 | 227 | PF00082 | 0.596 |
CLV_PCSK_KEX2_1 | 241 | 243 | PF00082 | 0.585 |
CLV_PCSK_KEX2_1 | 248 | 250 | PF00082 | 0.619 |
CLV_PCSK_KEX2_1 | 277 | 279 | PF00082 | 0.698 |
CLV_PCSK_KEX2_1 | 287 | 289 | PF00082 | 0.709 |
CLV_PCSK_KEX2_1 | 83 | 85 | PF00082 | 0.622 |
CLV_PCSK_KEX2_1 | 97 | 99 | PF00082 | 0.558 |
CLV_PCSK_PC1ET2_1 | 158 | 160 | PF00082 | 0.664 |
CLV_PCSK_PC1ET2_1 | 241 | 243 | PF00082 | 0.543 |
CLV_PCSK_PC1ET2_1 | 277 | 279 | PF00082 | 0.649 |
CLV_PCSK_PC1ET2_1 | 287 | 289 | PF00082 | 0.590 |
CLV_PCSK_PC1ET2_1 | 83 | 85 | PF00082 | 0.609 |
CLV_PCSK_PC7_1 | 222 | 228 | PF00082 | 0.580 |
CLV_PCSK_PC7_1 | 79 | 85 | PF00082 | 0.487 |
CLV_PCSK_SKI1_1 | 155 | 159 | PF00082 | 0.665 |
CLV_PCSK_SKI1_1 | 161 | 165 | PF00082 | 0.613 |
CLV_PCSK_SKI1_1 | 226 | 230 | PF00082 | 0.596 |
CLV_PCSK_SKI1_1 | 234 | 238 | PF00082 | 0.605 |
CLV_PCSK_SKI1_1 | 242 | 246 | PF00082 | 0.530 |
CLV_PCSK_SKI1_1 | 84 | 88 | PF00082 | 0.562 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.636 |
DOC_CKS1_1 | 47 | 52 | PF01111 | 0.585 |
DOC_MAPK_gen_1 | 207 | 216 | PF00069 | 0.624 |
DOC_MAPK_gen_1 | 30 | 39 | PF00069 | 0.559 |
DOC_MAPK_JIP1_4 | 208 | 214 | PF00069 | 0.537 |
DOC_MAPK_MEF2A_6 | 207 | 216 | PF00069 | 0.624 |
DOC_PP2B_LxvP_1 | 122 | 125 | PF13499 | 0.630 |
DOC_PP4_FxxP_1 | 33 | 36 | PF00568 | 0.586 |
DOC_USP7_MATH_1 | 106 | 110 | PF00917 | 0.628 |
DOC_USP7_MATH_1 | 125 | 129 | PF00917 | 0.645 |
DOC_USP7_MATH_1 | 174 | 178 | PF00917 | 0.612 |
DOC_USP7_MATH_1 | 192 | 196 | PF00917 | 0.664 |
DOC_USP7_MATH_1 | 218 | 222 | PF00917 | 0.726 |
DOC_USP7_MATH_1 | 28 | 32 | PF00917 | 0.592 |
DOC_USP7_UBL2_3 | 144 | 148 | PF12436 | 0.674 |
DOC_USP7_UBL2_3 | 151 | 155 | PF12436 | 0.608 |
DOC_USP7_UBL2_3 | 158 | 162 | PF12436 | 0.539 |
DOC_USP7_UBL2_3 | 264 | 268 | PF12436 | 0.593 |
DOC_USP7_UBL2_3 | 53 | 57 | PF12436 | 0.556 |
DOC_USP7_UBL2_3 | 83 | 87 | PF12436 | 0.508 |
DOC_WW_Pin1_4 | 15 | 20 | PF00397 | 0.593 |
DOC_WW_Pin1_4 | 242 | 247 | PF00397 | 0.562 |
DOC_WW_Pin1_4 | 46 | 51 | PF00397 | 0.600 |
LIG_14-3-3_CanoR_1 | 142 | 148 | PF00244 | 0.571 |
LIG_14-3-3_CanoR_1 | 161 | 169 | PF00244 | 0.600 |
LIG_14-3-3_CanoR_1 | 176 | 180 | PF00244 | 0.650 |
LIG_14-3-3_CanoR_1 | 225 | 233 | PF00244 | 0.614 |
LIG_Actin_WH2_2 | 150 | 166 | PF00022 | 0.599 |
LIG_BIR_III_2 | 25 | 29 | PF00653 | 0.566 |
LIG_FHA_1 | 124 | 130 | PF00498 | 0.714 |
LIG_FHA_1 | 88 | 94 | PF00498 | 0.558 |
LIG_FHA_2 | 47 | 53 | PF00498 | 0.664 |
LIG_LIR_Apic_2 | 31 | 36 | PF02991 | 0.586 |
LIG_RPA_C_Fungi | 74 | 86 | PF08784 | 0.483 |
LIG_SH2_STAT5 | 21 | 24 | PF00017 | 0.596 |
LIG_SH3_1 | 130 | 136 | PF00018 | 0.654 |
LIG_SH3_3 | 130 | 136 | PF00018 | 0.597 |
LIG_SH3_3 | 198 | 204 | PF00018 | 0.672 |
LIG_SH3_3 | 241 | 247 | PF00018 | 0.575 |
LIG_SH3_3 | 248 | 254 | PF00018 | 0.612 |
LIG_SH3_3 | 255 | 261 | PF00018 | 0.716 |
LIG_SUMO_SIM_par_1 | 120 | 126 | PF11976 | 0.539 |
LIG_SUMO_SIM_par_1 | 41 | 49 | PF11976 | 0.602 |
LIG_TRAF2_1 | 49 | 52 | PF00917 | 0.586 |
LIG_TRAF2_1 | 6 | 9 | PF00917 | 0.631 |
LIG_TRAF2_1 | 65 | 68 | PF00917 | 0.382 |
LIG_WW_3 | 245 | 249 | PF00397 | 0.528 |
MOD_CDK_SPxK_1 | 242 | 248 | PF00069 | 0.534 |
MOD_CDK_SPxxK_3 | 242 | 249 | PF00069 | 0.535 |
MOD_CDK_SPxxK_3 | 46 | 53 | PF00069 | 0.586 |
MOD_CK1_1 | 123 | 129 | PF00069 | 0.638 |
MOD_CK1_1 | 13 | 19 | PF00069 | 0.511 |
MOD_CK1_1 | 146 | 152 | PF00069 | 0.659 |
MOD_CK1_1 | 178 | 184 | PF00069 | 0.678 |
MOD_CK1_1 | 263 | 269 | PF00069 | 0.546 |
MOD_CK2_1 | 3 | 9 | PF00069 | 0.547 |
MOD_CK2_1 | 38 | 44 | PF00069 | 0.627 |
MOD_CK2_1 | 46 | 52 | PF00069 | 0.575 |
MOD_Cter_Amidation | 111 | 114 | PF01082 | 0.572 |
MOD_Cter_Amidation | 159 | 162 | PF01082 | 0.626 |
MOD_Cter_Amidation | 223 | 226 | PF01082 | 0.576 |
MOD_DYRK1A_RPxSP_1 | 242 | 246 | PF00069 | 0.537 |
MOD_GlcNHglycan | 5 | 8 | PF01048 | 0.555 |
MOD_GSK3_1 | 13 | 20 | PF00069 | 0.568 |
MOD_GSK3_1 | 174 | 181 | PF00069 | 0.647 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.517 |
MOD_NEK2_1 | 138 | 143 | PF00069 | 0.627 |
MOD_NEK2_1 | 163 | 168 | PF00069 | 0.601 |
MOD_NEK2_1 | 262 | 267 | PF00069 | 0.563 |
MOD_NEK2_2 | 125 | 130 | PF00069 | 0.613 |
MOD_NEK2_2 | 194 | 199 | PF00069 | 0.600 |
MOD_PIKK_1 | 10 | 16 | PF00454 | 0.566 |
MOD_PIKK_1 | 149 | 155 | PF00454 | 0.519 |
MOD_PKA_1 | 226 | 232 | PF00069 | 0.565 |
MOD_PKA_2 | 175 | 181 | PF00069 | 0.599 |
MOD_PKA_2 | 185 | 191 | PF00069 | 0.628 |
MOD_PKA_2 | 226 | 232 | PF00069 | 0.680 |
MOD_PKB_1 | 225 | 233 | PF00069 | 0.663 |
MOD_Plk_1 | 149 | 155 | PF00069 | 0.519 |
MOD_Plk_1 | 58 | 64 | PF00069 | 0.492 |
MOD_Plk_4 | 17 | 23 | PF00069 | 0.658 |
MOD_Plk_4 | 175 | 181 | PF00069 | 0.562 |
MOD_ProDKin_1 | 15 | 21 | PF00069 | 0.596 |
MOD_ProDKin_1 | 242 | 248 | PF00069 | 0.563 |
MOD_ProDKin_1 | 46 | 52 | PF00069 | 0.597 |
MOD_SUMO_for_1 | 147 | 150 | PF00179 | 0.649 |
TRG_ER_diArg_1 | 182 | 184 | PF00400 | 0.587 |
TRG_ER_diArg_1 | 207 | 209 | PF00400 | 0.797 |
TRG_ER_diArg_1 | 225 | 227 | PF00400 | 0.647 |
TRG_ER_diArg_1 | 247 | 249 | PF00400 | 0.549 |
TRG_ER_diArg_1 | 29 | 32 | PF00400 | 0.560 |
TRG_ER_diArg_1 | 97 | 99 | PF00400 | 0.640 |
TRG_ER_diLys_1 | 287 | 291 | PF00400 | 0.560 |
TRG_NLS_Bipartite_1 | 207 | 226 | PF00514 | 0.545 |
TRG_NLS_MonoExtC_3 | 157 | 162 | PF00514 | 0.666 |
TRG_NLS_MonoExtC_3 | 221 | 226 | PF00514 | 0.553 |
TRG_NLS_MonoExtC_3 | 82 | 87 | PF00514 | 0.503 |
TRG_NLS_MonoExtN_4 | 155 | 162 | PF00514 | 0.665 |
TRG_NLS_MonoExtN_4 | 275 | 280 | PF00514 | 0.520 |
TRG_NLS_MonoExtN_4 | 83 | 88 | PF00514 | 0.514 |
TRG_Pf-PMV_PEXEL_1 | 170 | 175 | PF00026 | 0.783 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7WW27 | Leishmania donovani | 79% | 100% |
A4HYU9 | Leishmania infantum | 80% | 100% |
E9AIF6 | Leishmania braziliensis | 54% | 100% |
E9AUP6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 75% | 100% |