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: 11 |
NetGPI | no | yes: 0, no: 11 |
Related structures:
AlphaFold database: A4HHJ0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 216 | 218 | PF00675 | 0.445 |
CLV_NRD_NRD_1 | 432 | 434 | PF00675 | 0.652 |
CLV_NRD_NRD_1 | 6 | 8 | PF00675 | 0.558 |
CLV_PCSK_KEX2_1 | 216 | 218 | PF00082 | 0.445 |
CLV_PCSK_KEX2_1 | 405 | 407 | PF00082 | 0.656 |
CLV_PCSK_KEX2_1 | 432 | 434 | PF00082 | 0.725 |
CLV_PCSK_PC1ET2_1 | 405 | 407 | PF00082 | 0.701 |
CLV_PCSK_SKI1_1 | 194 | 198 | PF00082 | 0.453 |
CLV_PCSK_SKI1_1 | 334 | 338 | PF00082 | 0.677 |
CLV_PCSK_SKI1_1 | 377 | 381 | PF00082 | 0.720 |
DEG_APCC_DBOX_1 | 333 | 341 | PF00400 | 0.719 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.624 |
DEG_SPOP_SBC_1 | 100 | 104 | PF00917 | 0.653 |
DEG_SPOP_SBC_1 | 246 | 250 | PF00917 | 0.717 |
DOC_CKS1_1 | 23 | 28 | PF01111 | 0.497 |
DOC_CKS1_1 | 323 | 328 | PF01111 | 0.644 |
DOC_MAPK_gen_1 | 7 | 15 | PF00069 | 0.546 |
DOC_MAPK_HePTP_8 | 30 | 42 | PF00069 | 0.426 |
DOC_MAPK_MEF2A_6 | 33 | 42 | PF00069 | 0.481 |
DOC_MAPK_MEF2A_6 | 8 | 17 | PF00069 | 0.485 |
DOC_PP2B_LxvP_1 | 42 | 45 | PF13499 | 0.375 |
DOC_PP2B_LxvP_1 | 434 | 437 | PF13499 | 0.729 |
DOC_PP4_FxxP_1 | 379 | 382 | PF00568 | 0.679 |
DOC_USP7_MATH_1 | 101 | 105 | PF00917 | 0.533 |
DOC_USP7_MATH_1 | 110 | 114 | PF00917 | 0.398 |
DOC_USP7_MATH_1 | 117 | 121 | PF00917 | 0.578 |
DOC_USP7_MATH_1 | 180 | 184 | PF00917 | 0.520 |
DOC_USP7_MATH_1 | 246 | 250 | PF00917 | 0.678 |
DOC_USP7_MATH_1 | 278 | 282 | PF00917 | 0.576 |
DOC_USP7_MATH_1 | 29 | 33 | PF00917 | 0.504 |
DOC_USP7_MATH_1 | 307 | 311 | PF00917 | 0.704 |
DOC_USP7_MATH_1 | 315 | 319 | PF00917 | 0.723 |
DOC_USP7_MATH_1 | 438 | 442 | PF00917 | 0.763 |
DOC_USP7_MATH_1 | 96 | 100 | PF00917 | 0.521 |
DOC_USP7_UBL2_3 | 381 | 385 | PF12436 | 0.668 |
DOC_WW_Pin1_4 | 22 | 27 | PF00397 | 0.508 |
DOC_WW_Pin1_4 | 322 | 327 | PF00397 | 0.675 |
DOC_WW_Pin1_4 | 343 | 348 | PF00397 | 0.687 |
LIG_14-3-3_CanoR_1 | 124 | 129 | PF00244 | 0.471 |
LIG_14-3-3_CanoR_1 | 279 | 285 | PF00244 | 0.631 |
LIG_14-3-3_CanoR_1 | 331 | 337 | PF00244 | 0.617 |
LIG_14-3-3_CanoR_1 | 82 | 90 | PF00244 | 0.388 |
LIG_BIR_III_4 | 154 | 158 | PF00653 | 0.378 |
LIG_BIR_III_4 | 161 | 165 | PF00653 | 0.245 |
LIG_BIR_III_4 | 264 | 268 | PF00653 | 0.391 |
LIG_BRCT_BRCA1_1 | 13 | 17 | PF00533 | 0.587 |
LIG_deltaCOP1_diTrp_1 | 202 | 210 | PF00928 | 0.547 |
LIG_deltaCOP1_diTrp_1 | 63 | 69 | PF00928 | 0.291 |
LIG_deltaCOP1_diTrp_1 | 9 | 18 | PF00928 | 0.445 |
LIG_eIF4E_1 | 195 | 201 | PF01652 | 0.312 |
LIG_FHA_1 | 106 | 112 | PF00498 | 0.692 |
LIG_FHA_1 | 275 | 281 | PF00498 | 0.577 |
LIG_FHA_1 | 285 | 291 | PF00498 | 0.677 |
LIG_FHA_1 | 399 | 405 | PF00498 | 0.648 |
LIG_FHA_1 | 409 | 415 | PF00498 | 0.583 |
LIG_FHA_1 | 426 | 432 | PF00498 | 0.519 |
LIG_FHA_1 | 45 | 51 | PF00498 | 0.472 |
LIG_LIR_Gen_1 | 136 | 146 | PF02991 | 0.375 |
LIG_LIR_Gen_1 | 66 | 76 | PF02991 | 0.404 |
LIG_LIR_Gen_1 | 81 | 91 | PF02991 | 0.377 |
LIG_LIR_Nem_3 | 136 | 141 | PF02991 | 0.367 |
LIG_LIR_Nem_3 | 191 | 196 | PF02991 | 0.490 |
LIG_LIR_Nem_3 | 66 | 72 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 81 | 86 | PF02991 | 0.379 |
LIG_PTB_Apo_2 | 335 | 342 | PF02174 | 0.688 |
LIG_SH2_CRK | 193 | 197 | PF00017 | 0.383 |
LIG_SH2_NCK_1 | 28 | 32 | PF00017 | 0.551 |
LIG_SH2_PTP2 | 174 | 177 | PF00017 | 0.524 |
LIG_SH2_SRC | 174 | 177 | PF00017 | 0.524 |
LIG_SH2_SRC | 221 | 224 | PF00017 | 0.365 |
LIG_SH2_STAP1 | 375 | 379 | PF00017 | 0.644 |
LIG_SH2_STAT5 | 138 | 141 | PF00017 | 0.359 |
LIG_SH2_STAT5 | 174 | 177 | PF00017 | 0.477 |
LIG_SH2_STAT5 | 195 | 198 | PF00017 | 0.419 |
LIG_SH2_STAT5 | 221 | 224 | PF00017 | 0.505 |
LIG_SH2_STAT5 | 409 | 412 | PF00017 | 0.553 |
LIG_SH3_3 | 174 | 180 | PF00018 | 0.540 |
LIG_SH3_3 | 320 | 326 | PF00018 | 0.678 |
LIG_SH3_4 | 381 | 388 | PF00018 | 0.692 |
LIG_SUMO_SIM_anti_2 | 413 | 419 | PF11976 | 0.663 |
LIG_SUMO_SIM_par_1 | 411 | 419 | PF11976 | 0.663 |
LIG_WRC_WIRS_1 | 316 | 321 | PF05994 | 0.746 |
LIG_WRC_WIRS_1 | 333 | 338 | PF05994 | 0.472 |
MOD_CDK_SPxxK_3 | 343 | 350 | PF00069 | 0.682 |
MOD_CK1_1 | 250 | 256 | PF00069 | 0.638 |
MOD_CK1_1 | 343 | 349 | PF00069 | 0.501 |
MOD_CK1_1 | 99 | 105 | PF00069 | 0.636 |
MOD_CK2_1 | 245 | 251 | PF00069 | 0.700 |
MOD_GlcNHglycan | 119 | 122 | PF01048 | 0.541 |
MOD_GlcNHglycan | 257 | 260 | PF01048 | 0.724 |
MOD_GlcNHglycan | 280 | 283 | PF01048 | 0.553 |
MOD_GlcNHglycan | 295 | 298 | PF01048 | 0.646 |
MOD_GlcNHglycan | 309 | 312 | PF01048 | 0.534 |
MOD_GlcNHglycan | 366 | 369 | PF01048 | 0.458 |
MOD_GlcNHglycan | 392 | 395 | PF01048 | 0.709 |
MOD_GlcNHglycan | 66 | 69 | PF01048 | 0.504 |
MOD_GlcNHglycan | 98 | 101 | PF01048 | 0.615 |
MOD_GSK3_1 | 105 | 112 | PF00069 | 0.611 |
MOD_GSK3_1 | 18 | 25 | PF00069 | 0.480 |
MOD_GSK3_1 | 205 | 212 | PF00069 | 0.483 |
MOD_GSK3_1 | 246 | 253 | PF00069 | 0.519 |
MOD_GSK3_1 | 274 | 281 | PF00069 | 0.505 |
MOD_GSK3_1 | 284 | 291 | PF00069 | 0.598 |
MOD_GSK3_1 | 325 | 332 | PF00069 | 0.630 |
MOD_GSK3_1 | 336 | 343 | PF00069 | 0.628 |
MOD_GSK3_1 | 438 | 445 | PF00069 | 0.783 |
MOD_GSK3_1 | 64 | 71 | PF00069 | 0.482 |
MOD_GSK3_1 | 96 | 103 | PF00069 | 0.571 |
MOD_N-GLC_1 | 253 | 258 | PF02516 | 0.668 |
MOD_N-GLC_1 | 291 | 296 | PF02516 | 0.560 |
MOD_NEK2_1 | 18 | 23 | PF00069 | 0.493 |
MOD_NEK2_1 | 200 | 205 | PF00069 | 0.424 |
MOD_NEK2_1 | 293 | 298 | PF00069 | 0.723 |
MOD_NEK2_1 | 336 | 341 | PF00069 | 0.693 |
MOD_NEK2_2 | 425 | 430 | PF00069 | 0.509 |
MOD_PIKK_1 | 2 | 8 | PF00454 | 0.574 |
MOD_PIKK_1 | 44 | 50 | PF00454 | 0.475 |
MOD_PKA_2 | 117 | 123 | PF00069 | 0.561 |
MOD_PKA_2 | 278 | 284 | PF00069 | 0.629 |
MOD_PKA_2 | 425 | 431 | PF00069 | 0.614 |
MOD_PKA_2 | 81 | 87 | PF00069 | 0.439 |
MOD_PKA_2 | 91 | 97 | PF00069 | 0.513 |
MOD_PKB_1 | 22 | 30 | PF00069 | 0.499 |
MOD_Plk_1 | 329 | 335 | PF00069 | 0.686 |
MOD_Plk_4 | 110 | 116 | PF00069 | 0.659 |
MOD_Plk_4 | 180 | 186 | PF00069 | 0.525 |
MOD_Plk_4 | 200 | 206 | PF00069 | 0.505 |
MOD_Plk_4 | 336 | 342 | PF00069 | 0.640 |
MOD_ProDKin_1 | 22 | 28 | PF00069 | 0.505 |
MOD_ProDKin_1 | 322 | 328 | PF00069 | 0.670 |
MOD_ProDKin_1 | 343 | 349 | PF00069 | 0.682 |
MOD_SUMO_for_1 | 380 | 383 | PF00179 | 0.706 |
MOD_SUMO_for_1 | 404 | 407 | PF00179 | 0.720 |
TRG_DiLeu_BaEn_1 | 166 | 171 | PF01217 | 0.371 |
TRG_DiLeu_BaEn_1 | 235 | 240 | PF01217 | 0.398 |
TRG_ENDOCYTIC_2 | 138 | 141 | PF00928 | 0.360 |
TRG_ENDOCYTIC_2 | 174 | 177 | PF00928 | 0.497 |
TRG_ENDOCYTIC_2 | 193 | 196 | PF00928 | 0.507 |
TRG_ER_diArg_1 | 216 | 218 | PF00400 | 0.446 |
TRG_ER_diArg_1 | 431 | 433 | PF00400 | 0.700 |
TRG_Pf-PMV_PEXEL_1 | 216 | 220 | PF00026 | 0.484 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2Q6 | Leptomonas seymouri | 65% | 95% |
A0A0S4KK06 | Bodo saltans | 26% | 92% |
A0A1X0NJ10 | Trypanosomatidae | 34% | 100% |
A0A3Q8IRG7 | Leishmania donovani | 87% | 100% |
A0A3R7NSU2 | Trypanosoma rangeli | 35% | 100% |
A4I4P8 | Leishmania infantum | 87% | 100% |
C9ZN48 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
E9AE51 | Leishmania major | 88% | 100% |
E9ALN4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
V5BIJ5 | Trypanosoma cruzi | 34% | 100% |