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: 8 |
NetGPI | no | yes: 0, no: 8 |
Related structures:
AlphaFold database: A0A3S5H7F3
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 120 | 124 | PF00656 | 0.570 |
CLV_C14_Caspase3-7 | 255 | 259 | PF00656 | 0.529 |
CLV_C14_Caspase3-7 | 280 | 284 | PF00656 | 0.466 |
CLV_C14_Caspase3-7 | 3 | 7 | PF00656 | 0.572 |
CLV_NRD_NRD_1 | 32 | 34 | PF00675 | 0.516 |
CLV_NRD_NRD_1 | 328 | 330 | PF00675 | 0.460 |
CLV_NRD_NRD_1 | 339 | 341 | PF00675 | 0.377 |
CLV_NRD_NRD_1 | 344 | 346 | PF00675 | 0.402 |
CLV_NRD_NRD_1 | 49 | 51 | PF00675 | 0.423 |
CLV_PCSK_KEX2_1 | 171 | 173 | PF00082 | 0.556 |
CLV_PCSK_KEX2_1 | 272 | 274 | PF00082 | 0.462 |
CLV_PCSK_KEX2_1 | 32 | 34 | PF00082 | 0.516 |
CLV_PCSK_KEX2_1 | 328 | 330 | PF00082 | 0.433 |
CLV_PCSK_KEX2_1 | 338 | 340 | PF00082 | 0.373 |
CLV_PCSK_KEX2_1 | 48 | 50 | PF00082 | 0.435 |
CLV_PCSK_KEX2_1 | 8 | 10 | PF00082 | 0.520 |
CLV_PCSK_PC1ET2_1 | 171 | 173 | PF00082 | 0.556 |
CLV_PCSK_PC1ET2_1 | 272 | 274 | PF00082 | 0.482 |
CLV_PCSK_PC1ET2_1 | 8 | 10 | PF00082 | 0.520 |
CLV_PCSK_SKI1_1 | 168 | 172 | PF00082 | 0.569 |
CLV_PCSK_SKI1_1 | 220 | 224 | PF00082 | 0.583 |
CLV_PCSK_SKI1_1 | 339 | 343 | PF00082 | 0.422 |
CLV_PCSK_SKI1_1 | 5 | 9 | PF00082 | 0.550 |
DEG_SIAH_1 | 16 | 24 | PF03145 | 0.506 |
DOC_CDC14_PxL_1 | 78 | 86 | PF14671 | 0.628 |
DOC_PP2B_LxvP_1 | 84 | 87 | PF13499 | 0.611 |
DOC_PP4_FxxP_1 | 170 | 173 | PF00568 | 0.513 |
DOC_PP4_FxxP_1 | 263 | 266 | PF00568 | 0.481 |
DOC_USP7_MATH_1 | 100 | 104 | PF00917 | 0.673 |
DOC_USP7_MATH_1 | 175 | 179 | PF00917 | 0.595 |
DOC_USP7_MATH_1 | 241 | 245 | PF00917 | 0.552 |
DOC_USP7_UBL2_3 | 342 | 346 | PF12436 | 0.566 |
DOC_WW_Pin1_4 | 130 | 135 | PF00397 | 0.516 |
DOC_WW_Pin1_4 | 178 | 183 | PF00397 | 0.635 |
DOC_WW_Pin1_4 | 60 | 65 | PF00397 | 0.641 |
LIG_14-3-3_CanoR_1 | 220 | 229 | PF00244 | 0.545 |
LIG_14-3-3_CanoR_1 | 240 | 246 | PF00244 | 0.395 |
LIG_14-3-3_CanoR_1 | 254 | 263 | PF00244 | 0.548 |
LIG_14-3-3_CanoR_1 | 345 | 349 | PF00244 | 0.485 |
LIG_14-3-3_CanoR_1 | 85 | 91 | PF00244 | 0.519 |
LIG_Actin_WH2_2 | 140 | 158 | PF00022 | 0.388 |
LIG_BRCT_BRCA1_1 | 180 | 184 | PF00533 | 0.513 |
LIG_BRCT_BRCA1_1 | 25 | 29 | PF00533 | 0.509 |
LIG_FHA_1 | 194 | 200 | PF00498 | 0.590 |
LIG_FHA_1 | 260 | 266 | PF00498 | 0.584 |
LIG_FHA_2 | 158 | 164 | PF00498 | 0.511 |
LIG_FHA_2 | 202 | 208 | PF00498 | 0.502 |
LIG_FHA_2 | 253 | 259 | PF00498 | 0.534 |
LIG_FHA_2 | 68 | 74 | PF00498 | 0.601 |
LIG_GBD_Chelix_1 | 111 | 119 | PF00786 | 0.546 |
LIG_LIR_Apic_2 | 167 | 173 | PF02991 | 0.505 |
LIG_LIR_Apic_2 | 261 | 266 | PF02991 | 0.484 |
LIG_LIR_Nem_3 | 214 | 218 | PF02991 | 0.481 |
LIG_NRBOX | 302 | 308 | PF00104 | 0.428 |
LIG_Rb_pABgroove_1 | 23 | 31 | PF01858 | 0.512 |
LIG_SH2_CRK | 14 | 18 | PF00017 | 0.534 |
LIG_SH2_NCK_1 | 97 | 101 | PF00017 | 0.453 |
LIG_SH2_PTP2 | 296 | 299 | PF00017 | 0.483 |
LIG_SH2_SRC | 97 | 100 | PF00017 | 0.473 |
LIG_SH2_STAP1 | 218 | 222 | PF00017 | 0.505 |
LIG_SH2_STAP1 | 245 | 249 | PF00017 | 0.627 |
LIG_SH2_STAP1 | 275 | 279 | PF00017 | 0.486 |
LIG_SH2_STAP1 | 95 | 99 | PF00017 | 0.532 |
LIG_SH2_STAT5 | 296 | 299 | PF00017 | 0.489 |
LIG_SH3_3 | 17 | 23 | PF00018 | 0.408 |
LIG_SH3_3 | 176 | 182 | PF00018 | 0.567 |
LIG_SH3_3 | 62 | 68 | PF00018 | 0.779 |
LIG_SUMO_SIM_anti_2 | 108 | 113 | PF11976 | 0.429 |
LIG_SUMO_SIM_anti_2 | 300 | 309 | PF11976 | 0.529 |
LIG_SUMO_SIM_par_1 | 276 | 283 | PF11976 | 0.467 |
LIG_TRAF2_1 | 211 | 214 | PF00917 | 0.478 |
LIG_WRC_WIRS_1 | 24 | 29 | PF05994 | 0.512 |
MOD_CK1_1 | 124 | 130 | PF00069 | 0.643 |
MOD_CK1_1 | 133 | 139 | PF00069 | 0.444 |
MOD_CK1_1 | 178 | 184 | PF00069 | 0.758 |
MOD_CK1_1 | 243 | 249 | PF00069 | 0.576 |
MOD_CK1_1 | 60 | 66 | PF00069 | 0.726 |
MOD_CK2_1 | 161 | 167 | PF00069 | 0.643 |
MOD_CK2_1 | 222 | 228 | PF00069 | 0.472 |
MOD_CK2_1 | 60 | 66 | PF00069 | 0.609 |
MOD_GlcNHglycan | 267 | 270 | PF01048 | 0.509 |
MOD_GlcNHglycan | 60 | 63 | PF01048 | 0.637 |
MOD_GSK3_1 | 117 | 124 | PF00069 | 0.593 |
MOD_GSK3_1 | 125 | 132 | PF00069 | 0.720 |
MOD_GSK3_1 | 157 | 164 | PF00069 | 0.582 |
MOD_GSK3_1 | 254 | 261 | PF00069 | 0.650 |
MOD_GSK3_1 | 34 | 41 | PF00069 | 0.460 |
MOD_GSK3_1 | 76 | 83 | PF00069 | 0.521 |
MOD_N-GLC_1 | 101 | 106 | PF02516 | 0.640 |
MOD_N-GLC_1 | 124 | 129 | PF02516 | 0.467 |
MOD_N-GLC_1 | 241 | 246 | PF02516 | 0.468 |
MOD_NEK2_1 | 161 | 166 | PF00069 | 0.645 |
MOD_NEK2_1 | 199 | 204 | PF00069 | 0.531 |
MOD_NEK2_1 | 221 | 226 | PF00069 | 0.500 |
MOD_NEK2_1 | 229 | 234 | PF00069 | 0.579 |
MOD_NEK2_1 | 34 | 39 | PF00069 | 0.414 |
MOD_PIKK_1 | 126 | 132 | PF00454 | 0.590 |
MOD_PIKK_1 | 133 | 139 | PF00454 | 0.484 |
MOD_PKA_2 | 344 | 350 | PF00069 | 0.390 |
MOD_Plk_1 | 107 | 113 | PF00069 | 0.675 |
MOD_Plk_1 | 161 | 167 | PF00069 | 0.600 |
MOD_Plk_1 | 175 | 181 | PF00069 | 0.547 |
MOD_Plk_1 | 241 | 247 | PF00069 | 0.612 |
MOD_Plk_1 | 34 | 40 | PF00069 | 0.498 |
MOD_Plk_2-3 | 157 | 163 | PF00069 | 0.497 |
MOD_Plk_2-3 | 277 | 283 | PF00069 | 0.468 |
MOD_Plk_2-3 | 309 | 315 | PF00069 | 0.436 |
MOD_Plk_4 | 107 | 113 | PF00069 | 0.672 |
MOD_Plk_4 | 117 | 123 | PF00069 | 0.561 |
MOD_Plk_4 | 138 | 144 | PF00069 | 0.516 |
MOD_Plk_4 | 23 | 29 | PF00069 | 0.448 |
MOD_Plk_4 | 259 | 265 | PF00069 | 0.641 |
MOD_Plk_4 | 34 | 40 | PF00069 | 0.404 |
MOD_ProDKin_1 | 130 | 136 | PF00069 | 0.505 |
MOD_ProDKin_1 | 178 | 184 | PF00069 | 0.638 |
MOD_ProDKin_1 | 60 | 66 | PF00069 | 0.644 |
MOD_SUMO_rev_2 | 224 | 232 | PF00179 | 0.480 |
MOD_SUMO_rev_2 | 253 | 262 | PF00179 | 0.588 |
TRG_DiLeu_BaEn_4 | 276 | 282 | PF01217 | 0.468 |
TRG_DiLeu_BaLyEn_6 | 20 | 25 | PF01217 | 0.441 |
TRG_DiLeu_BaLyEn_6 | 217 | 222 | PF01217 | 0.457 |
TRG_ENDOCYTIC_2 | 218 | 221 | PF00928 | 0.533 |
TRG_ENDOCYTIC_2 | 275 | 278 | PF00928 | 0.403 |
TRG_ENDOCYTIC_2 | 296 | 299 | PF00928 | 0.483 |
TRG_ER_diArg_1 | 31 | 33 | PF00400 | 0.514 |
TRG_ER_diArg_1 | 337 | 340 | PF00400 | 0.389 |
TRG_ER_diArg_1 | 356 | 359 | PF00400 | 0.470 |
TRG_ER_diArg_1 | 47 | 50 | PF00400 | 0.422 |
TRG_NLS_MonoCore_2 | 170 | 175 | PF00514 | 0.584 |
TRG_NLS_MonoExtC_3 | 170 | 175 | PF00514 | 0.580 |
TRG_NLS_MonoExtN_4 | 168 | 175 | PF00514 | 0.524 |
TRG_Pf-PMV_PEXEL_1 | 339 | 343 | PF00026 | 0.388 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IKE1 | Leptomonas seymouri | 44% | 100% |
A0A1X0NZJ6 | Trypanosomatidae | 27% | 100% |
A0A3R7KZA5 | Trypanosoma rangeli | 26% | 91% |
A4HED8 | Leishmania braziliensis | 67% | 100% |
A4I1T5 | Leishmania infantum | 99% | 100% |
E9AXW9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |
Q4Q9K1 | Leishmania major | 86% | 100% |