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: 9 |
NetGPI | no | yes: 0, no: 9 |
Related structures:
AlphaFold database: A4HBD2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 212 | 216 | PF00656 | 0.634 |
CLV_C14_Caspase3-7 | 75 | 79 | PF00656 | 0.538 |
CLV_NRD_NRD_1 | 365 | 367 | PF00675 | 0.503 |
CLV_NRD_NRD_1 | 372 | 374 | PF00675 | 0.682 |
CLV_NRD_NRD_1 | 9 | 11 | PF00675 | 0.574 |
CLV_PCSK_FUR_1 | 363 | 367 | PF00082 | 0.384 |
CLV_PCSK_KEX2_1 | 112 | 114 | PF00082 | 0.588 |
CLV_PCSK_KEX2_1 | 365 | 367 | PF00082 | 0.407 |
CLV_PCSK_KEX2_1 | 372 | 374 | PF00082 | 0.590 |
CLV_PCSK_PC1ET2_1 | 112 | 114 | PF00082 | 0.583 |
CLV_PCSK_SKI1_1 | 19 | 23 | PF00082 | 0.670 |
CLV_PCSK_SKI1_1 | 289 | 293 | PF00082 | 0.432 |
CLV_PCSK_SKI1_1 | 29 | 33 | PF00082 | 0.533 |
CLV_PCSK_SKI1_1 | 296 | 300 | PF00082 | 0.470 |
CLV_PCSK_SKI1_1 | 409 | 413 | PF00082 | 0.369 |
CLV_PCSK_SKI1_1 | 427 | 431 | PF00082 | 0.369 |
CLV_PCSK_SKI1_1 | 95 | 99 | PF00082 | 0.617 |
CLV_Separin_Metazoa | 360 | 364 | PF03568 | 0.370 |
DEG_APCC_DBOX_1 | 28 | 36 | PF00400 | 0.467 |
DEG_APCC_DBOX_1 | 408 | 416 | PF00400 | 0.444 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.549 |
DOC_CYCLIN_RxL_1 | 286 | 294 | PF00134 | 0.492 |
DOC_CYCLIN_RxL_1 | 406 | 416 | PF00134 | 0.401 |
DOC_MAPK_DCC_7 | 29 | 37 | PF00069 | 0.648 |
DOC_MAPK_gen_1 | 363 | 371 | PF00069 | 0.592 |
DOC_MAPK_MEF2A_6 | 29 | 37 | PF00069 | 0.648 |
DOC_PP2B_LxvP_1 | 154 | 157 | PF13499 | 0.457 |
DOC_USP7_MATH_1 | 224 | 228 | PF00917 | 0.533 |
DOC_USP7_MATH_1 | 240 | 244 | PF00917 | 0.684 |
DOC_USP7_MATH_1 | 318 | 322 | PF00917 | 0.760 |
DOC_USP7_MATH_1 | 50 | 54 | PF00917 | 0.510 |
DOC_USP7_UBL2_3 | 427 | 431 | PF12436 | 0.339 |
DOC_WW_Pin1_4 | 80 | 85 | PF00397 | 0.690 |
LIG_14-3-3_CanoR_1 | 372 | 378 | PF00244 | 0.488 |
LIG_14-3-3_CanoR_1 | 397 | 403 | PF00244 | 0.364 |
LIG_Actin_WH2_2 | 337 | 355 | PF00022 | 0.417 |
LIG_Actin_WH2_2 | 404 | 422 | PF00022 | 0.444 |
LIG_Actin_WH2_2 | 90 | 107 | PF00022 | 0.582 |
LIG_BRCT_BRCA1_1 | 350 | 354 | PF00533 | 0.388 |
LIG_CaM_IQ_9 | 90 | 105 | PF13499 | 0.624 |
LIG_FHA_1 | 113 | 119 | PF00498 | 0.616 |
LIG_FHA_1 | 120 | 126 | PF00498 | 0.566 |
LIG_FHA_1 | 7 | 13 | PF00498 | 0.545 |
LIG_FHA_2 | 138 | 144 | PF00498 | 0.538 |
LIG_FHA_2 | 174 | 180 | PF00498 | 0.590 |
LIG_FHA_2 | 253 | 259 | PF00498 | 0.574 |
LIG_FHA_2 | 318 | 324 | PF00498 | 0.757 |
LIG_FHA_2 | 362 | 368 | PF00498 | 0.575 |
LIG_FHA_2 | 420 | 426 | PF00498 | 0.449 |
LIG_FHA_2 | 86 | 92 | PF00498 | 0.656 |
LIG_GBD_Chelix_1 | 394 | 402 | PF00786 | 0.485 |
LIG_LIR_Gen_1 | 257 | 267 | PF02991 | 0.515 |
LIG_LIR_Gen_1 | 328 | 337 | PF02991 | 0.599 |
LIG_LIR_Nem_3 | 257 | 263 | PF02991 | 0.503 |
LIG_LIR_Nem_3 | 328 | 334 | PF02991 | 0.613 |
LIG_LIR_Nem_3 | 351 | 357 | PF02991 | 0.606 |
LIG_NRBOX | 414 | 420 | PF00104 | 0.344 |
LIG_SH2_GRB2like | 260 | 263 | PF00017 | 0.382 |
LIG_SH2_SRC | 45 | 48 | PF00017 | 0.615 |
LIG_SH2_STAP1 | 191 | 195 | PF00017 | 0.522 |
LIG_SH2_STAP1 | 45 | 49 | PF00017 | 0.640 |
LIG_SH2_STAT3 | 36 | 39 | PF00017 | 0.681 |
LIG_SH2_STAT5 | 260 | 263 | PF00017 | 0.593 |
LIG_SH2_STAT5 | 36 | 39 | PF00017 | 0.647 |
LIG_SH2_STAT5 | 390 | 393 | PF00017 | 0.344 |
LIG_SH3_3 | 234 | 240 | PF00018 | 0.654 |
LIG_SUMO_SIM_par_1 | 4 | 9 | PF11976 | 0.549 |
LIG_TRAF2_2 | 68 | 73 | PF00917 | 0.655 |
LIG_UBA3_1 | 291 | 296 | PF00899 | 0.503 |
LIG_UBA3_1 | 411 | 420 | PF00899 | 0.444 |
MOD_CDC14_SPxK_1 | 83 | 86 | PF00782 | 0.544 |
MOD_CDK_SPxK_1 | 80 | 86 | PF00069 | 0.569 |
MOD_CK1_1 | 145 | 151 | PF00069 | 0.506 |
MOD_CK1_1 | 252 | 258 | PF00069 | 0.451 |
MOD_CK1_1 | 309 | 315 | PF00069 | 0.718 |
MOD_CK1_1 | 79 | 85 | PF00069 | 0.746 |
MOD_CK2_1 | 111 | 117 | PF00069 | 0.418 |
MOD_CK2_1 | 128 | 134 | PF00069 | 0.340 |
MOD_CK2_1 | 137 | 143 | PF00069 | 0.453 |
MOD_CK2_1 | 173 | 179 | PF00069 | 0.543 |
MOD_CK2_1 | 318 | 324 | PF00069 | 0.609 |
MOD_CK2_1 | 361 | 367 | PF00069 | 0.632 |
MOD_CK2_1 | 85 | 91 | PF00069 | 0.662 |
MOD_GlcNHglycan | 191 | 194 | PF01048 | 0.347 |
MOD_GlcNHglycan | 227 | 230 | PF01048 | 0.427 |
MOD_GlcNHglycan | 251 | 254 | PF01048 | 0.513 |
MOD_GlcNHglycan | 300 | 303 | PF01048 | 0.654 |
MOD_GlcNHglycan | 320 | 323 | PF01048 | 0.663 |
MOD_GlcNHglycan | 78 | 81 | PF01048 | 0.778 |
MOD_GSK3_1 | 137 | 144 | PF00069 | 0.443 |
MOD_GSK3_1 | 225 | 232 | PF00069 | 0.685 |
MOD_GSK3_1 | 308 | 315 | PF00069 | 0.694 |
MOD_GSK3_1 | 318 | 325 | PF00069 | 0.733 |
MOD_GSK3_1 | 372 | 379 | PF00069 | 0.614 |
MOD_GSK3_1 | 72 | 79 | PF00069 | 0.807 |
MOD_N-GLC_1 | 145 | 150 | PF02516 | 0.602 |
MOD_N-GLC_1 | 312 | 317 | PF02516 | 0.675 |
MOD_NEK2_1 | 111 | 116 | PF00069 | 0.456 |
MOD_NEK2_1 | 142 | 147 | PF00069 | 0.402 |
MOD_NEK2_1 | 173 | 178 | PF00069 | 0.573 |
MOD_NEK2_1 | 22 | 27 | PF00069 | 0.574 |
MOD_NEK2_1 | 361 | 366 | PF00069 | 0.509 |
MOD_NEK2_1 | 371 | 376 | PF00069 | 0.560 |
MOD_NEK2_1 | 398 | 403 | PF00069 | 0.414 |
MOD_PIKK_1 | 182 | 188 | PF00454 | 0.599 |
MOD_PIKK_1 | 322 | 328 | PF00454 | 0.725 |
MOD_PKA_1 | 112 | 118 | PF00069 | 0.618 |
MOD_PKA_1 | 372 | 378 | PF00069 | 0.718 |
MOD_PKA_2 | 112 | 118 | PF00069 | 0.610 |
MOD_PKA_2 | 137 | 143 | PF00069 | 0.510 |
MOD_PKA_2 | 182 | 188 | PF00069 | 0.482 |
MOD_PKA_2 | 371 | 377 | PF00069 | 0.553 |
MOD_PKA_2 | 85 | 91 | PF00069 | 0.511 |
MOD_Plk_1 | 128 | 134 | PF00069 | 0.638 |
MOD_Plk_1 | 145 | 151 | PF00069 | 0.524 |
MOD_Plk_1 | 173 | 179 | PF00069 | 0.424 |
MOD_Plk_1 | 22 | 28 | PF00069 | 0.648 |
MOD_Plk_1 | 312 | 318 | PF00069 | 0.658 |
MOD_Plk_1 | 348 | 354 | PF00069 | 0.484 |
MOD_Plk_1 | 56 | 62 | PF00069 | 0.653 |
MOD_Plk_4 | 414 | 420 | PF00069 | 0.366 |
MOD_Plk_4 | 50 | 56 | PF00069 | 0.507 |
MOD_Plk_4 | 85 | 91 | PF00069 | 0.515 |
MOD_ProDKin_1 | 80 | 86 | PF00069 | 0.684 |
MOD_SUMO_rev_2 | 160 | 165 | PF00179 | 0.600 |
MOD_SUMO_rev_2 | 265 | 270 | PF00179 | 0.466 |
MOD_SUMO_rev_2 | 423 | 429 | PF00179 | 0.344 |
TRG_DiLeu_BaEn_1 | 17 | 22 | PF01217 | 0.410 |
TRG_ENDOCYTIC_2 | 260 | 263 | PF00928 | 0.494 |
TRG_ENDOCYTIC_2 | 267 | 270 | PF00928 | 0.464 |
TRG_ER_diArg_1 | 175 | 178 | PF00400 | 0.575 |
TRG_ER_diArg_1 | 362 | 365 | PF00400 | 0.483 |
TRG_ER_diArg_1 | 371 | 373 | PF00400 | 0.688 |
TRG_Pf-PMV_PEXEL_1 | 10 | 14 | PF00026 | 0.560 |
TRG_Pf-PMV_PEXEL_1 | 19 | 23 | PF00026 | 0.648 |
TRG_Pf-PMV_PEXEL_1 | 293 | 297 | PF00026 | 0.570 |
TRG_Pf-PMV_PEXEL_1 | 345 | 349 | PF00026 | 0.587 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PF68 | Leptomonas seymouri | 42% | 92% |
A0A1X0PB65 | Trypanosomatidae | 25% | 95% |
A0A3S7X8J7 | Leishmania donovani | 66% | 100% |
A4IAI0 | Leishmania infantum | 66% | 89% |
C9ZLQ9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 94% |
E9B5K4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 64% | 100% |
Q4Q2D2 | Leishmania major | 64% | 100% |
V5BW28 | Trypanosoma cruzi | 27% | 92% |