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: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: Q95ZB6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 207 | 211 | PF00656 | 0.362 |
CLV_C14_Caspase3-7 | 368 | 372 | PF00656 | 0.536 |
CLV_NRD_NRD_1 | 148 | 150 | PF00675 | 0.462 |
CLV_NRD_NRD_1 | 45 | 47 | PF00675 | 0.561 |
CLV_NRD_NRD_1 | 505 | 507 | PF00675 | 0.490 |
CLV_NRD_NRD_1 | 98 | 100 | PF00675 | 0.474 |
CLV_PCSK_KEX2_1 | 148 | 150 | PF00082 | 0.462 |
CLV_PCSK_KEX2_1 | 373 | 375 | PF00082 | 0.545 |
CLV_PCSK_KEX2_1 | 45 | 47 | PF00082 | 0.561 |
CLV_PCSK_KEX2_1 | 505 | 507 | PF00082 | 0.492 |
CLV_PCSK_PC1ET2_1 | 373 | 375 | PF00082 | 0.415 |
CLV_PCSK_SKI1_1 | 115 | 119 | PF00082 | 0.386 |
CLV_PCSK_SKI1_1 | 148 | 152 | PF00082 | 0.407 |
CLV_PCSK_SKI1_1 | 29 | 33 | PF00082 | 0.464 |
CLV_PCSK_SKI1_1 | 309 | 313 | PF00082 | 0.432 |
CLV_PCSK_SKI1_1 | 468 | 472 | PF00082 | 0.452 |
DEG_APCC_DBOX_1 | 147 | 155 | PF00400 | 0.503 |
DEG_APCC_DBOX_1 | 467 | 475 | PF00400 | 0.356 |
DEG_SCF_TRCP1_1 | 532 | 538 | PF00400 | 0.482 |
DOC_CKS1_1 | 22 | 27 | PF01111 | 0.474 |
DOC_MAPK_gen_1 | 280 | 289 | PF00069 | 0.415 |
DOC_MAPK_MEF2A_6 | 230 | 238 | PF00069 | 0.487 |
DOC_MAPK_MEF2A_6 | 282 | 291 | PF00069 | 0.449 |
DOC_MAPK_MEF2A_6 | 425 | 432 | PF00069 | 0.449 |
DOC_PP1_RVXF_1 | 113 | 119 | PF00149 | 0.454 |
DOC_PP1_SILK_1 | 260 | 265 | PF00149 | 0.340 |
DOC_PP2B_LxvP_1 | 23 | 26 | PF13499 | 0.559 |
DOC_PP4_FxxP_1 | 526 | 529 | PF00568 | 0.694 |
DOC_USP7_MATH_1 | 12 | 16 | PF00917 | 0.469 |
DOC_USP7_MATH_1 | 127 | 131 | PF00917 | 0.516 |
DOC_USP7_MATH_1 | 158 | 162 | PF00917 | 0.372 |
DOC_USP7_MATH_1 | 384 | 388 | PF00917 | 0.436 |
DOC_USP7_MATH_1 | 44 | 48 | PF00917 | 0.493 |
DOC_USP7_MATH_1 | 535 | 539 | PF00917 | 0.668 |
DOC_USP7_UBL2_3 | 155 | 159 | PF12436 | 0.501 |
DOC_USP7_UBL2_3 | 571 | 575 | PF12436 | 0.491 |
DOC_USP7_UBL2_3 | 59 | 63 | PF12436 | 0.427 |
DOC_WW_Pin1_4 | 21 | 26 | PF00397 | 0.489 |
DOC_WW_Pin1_4 | 270 | 275 | PF00397 | 0.366 |
DOC_WW_Pin1_4 | 291 | 296 | PF00397 | 0.350 |
DOC_WW_Pin1_4 | 317 | 322 | PF00397 | 0.447 |
DOC_WW_Pin1_4 | 423 | 428 | PF00397 | 0.485 |
DOC_WW_Pin1_4 | 525 | 530 | PF00397 | 0.668 |
LIG_14-3-3_CanoR_1 | 29 | 37 | PF00244 | 0.613 |
LIG_14-3-3_CanoR_1 | 347 | 353 | PF00244 | 0.485 |
LIG_14-3-3_CanoR_1 | 45 | 53 | PF00244 | 0.407 |
LIG_Actin_WH2_2 | 140 | 157 | PF00022 | 0.443 |
LIG_Actin_WH2_2 | 453 | 470 | PF00022 | 0.373 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.578 |
LIG_BRCT_BRCA1_1 | 194 | 198 | PF00533 | 0.446 |
LIG_BRCT_BRCA1_1 | 448 | 452 | PF00533 | 0.511 |
LIG_EH_1 | 76 | 80 | PF12763 | 0.449 |
LIG_eIF4E_1 | 466 | 472 | PF01652 | 0.366 |
LIG_FHA_1 | 120 | 126 | PF00498 | 0.474 |
LIG_FHA_1 | 183 | 189 | PF00498 | 0.493 |
LIG_FHA_1 | 197 | 203 | PF00498 | 0.397 |
LIG_FHA_1 | 266 | 272 | PF00498 | 0.308 |
LIG_FHA_1 | 343 | 349 | PF00498 | 0.408 |
LIG_FHA_1 | 557 | 563 | PF00498 | 0.343 |
LIG_FHA_2 | 134 | 140 | PF00498 | 0.583 |
LIG_FHA_2 | 205 | 211 | PF00498 | 0.361 |
LIG_FHA_2 | 288 | 294 | PF00498 | 0.467 |
LIG_FHA_2 | 31 | 37 | PF00498 | 0.437 |
LIG_FHA_2 | 334 | 340 | PF00498 | 0.483 |
LIG_FHA_2 | 349 | 355 | PF00498 | 0.297 |
LIG_LIR_Apic_2 | 298 | 302 | PF02991 | 0.427 |
LIG_LIR_Apic_2 | 378 | 384 | PF02991 | 0.504 |
LIG_LIR_Gen_1 | 250 | 259 | PF02991 | 0.368 |
LIG_LIR_Gen_1 | 268 | 274 | PF02991 | 0.388 |
LIG_LIR_Gen_1 | 363 | 372 | PF02991 | 0.454 |
LIG_LIR_Gen_1 | 498 | 504 | PF02991 | 0.312 |
LIG_LIR_Gen_1 | 5 | 14 | PF02991 | 0.530 |
LIG_LIR_Nem_3 | 250 | 254 | PF02991 | 0.361 |
LIG_LIR_Nem_3 | 268 | 272 | PF02991 | 0.380 |
LIG_LIR_Nem_3 | 363 | 369 | PF02991 | 0.432 |
LIG_LIR_Nem_3 | 498 | 502 | PF02991 | 0.304 |
LIG_LIR_Nem_3 | 5 | 10 | PF02991 | 0.518 |
LIG_MLH1_MIPbox_1 | 448 | 452 | PF16413 | 0.511 |
LIG_Pex14_1 | 564 | 568 | PF04695 | 0.291 |
LIG_Pex14_2 | 447 | 451 | PF04695 | 0.497 |
LIG_SH2_CRK | 299 | 303 | PF00017 | 0.314 |
LIG_SH2_CRK | 318 | 322 | PF00017 | 0.452 |
LIG_SH2_CRK | 381 | 385 | PF00017 | 0.519 |
LIG_SH2_GRB2like | 572 | 575 | PF00017 | 0.298 |
LIG_SH2_NCK_1 | 318 | 322 | PF00017 | 0.452 |
LIG_SH2_SRC | 381 | 384 | PF00017 | 0.482 |
LIG_SH2_SRC | 393 | 396 | PF00017 | 0.342 |
LIG_SH2_STAP1 | 251 | 255 | PF00017 | 0.427 |
LIG_SH2_STAP1 | 30 | 34 | PF00017 | 0.363 |
LIG_SH2_STAP1 | 572 | 576 | PF00017 | 0.428 |
LIG_SH2_STAT3 | 85 | 88 | PF00017 | 0.503 |
LIG_SH2_STAT5 | 156 | 159 | PF00017 | 0.510 |
LIG_SH2_STAT5 | 265 | 268 | PF00017 | 0.323 |
LIG_SH2_STAT5 | 318 | 321 | PF00017 | 0.451 |
LIG_SH2_STAT5 | 466 | 469 | PF00017 | 0.351 |
LIG_SH3_3 | 159 | 165 | PF00018 | 0.451 |
LIG_SH3_3 | 19 | 25 | PF00018 | 0.452 |
LIG_SH3_3 | 268 | 274 | PF00018 | 0.379 |
LIG_SUMO_SIM_anti_2 | 17 | 24 | PF11976 | 0.527 |
LIG_SUMO_SIM_anti_2 | 252 | 258 | PF11976 | 0.269 |
LIG_SUMO_SIM_par_1 | 12 | 18 | PF11976 | 0.474 |
LIG_SUMO_SIM_par_1 | 252 | 258 | PF11976 | 0.336 |
LIG_SUMO_SIM_par_1 | 287 | 294 | PF11976 | 0.397 |
LIG_SUMO_SIM_par_1 | 492 | 498 | PF11976 | 0.430 |
LIG_TRAF2_1 | 483 | 486 | PF00917 | 0.379 |
LIG_UBA3_1 | 304 | 309 | PF00899 | 0.343 |
LIG_WRC_WIRS_1 | 266 | 271 | PF05994 | 0.314 |
LIG_WRC_WIRS_1 | 68 | 73 | PF05994 | 0.416 |
LIG_WW_1 | 508 | 511 | PF00397 | 0.524 |
MOD_CDK_SPK_2 | 270 | 275 | PF00069 | 0.397 |
MOD_CK1_1 | 15 | 21 | PF00069 | 0.477 |
MOD_CK1_1 | 48 | 54 | PF00069 | 0.526 |
MOD_CK1_1 | 528 | 534 | PF00069 | 0.696 |
MOD_CK1_1 | 538 | 544 | PF00069 | 0.571 |
MOD_CK1_1 | 546 | 552 | PF00069 | 0.449 |
MOD_CK2_1 | 287 | 293 | PF00069 | 0.355 |
MOD_CK2_1 | 30 | 36 | PF00069 | 0.447 |
MOD_CK2_1 | 333 | 339 | PF00069 | 0.525 |
MOD_GlcNHglycan | 105 | 108 | PF01048 | 0.390 |
MOD_GlcNHglycan | 26 | 29 | PF01048 | 0.573 |
MOD_GlcNHglycan | 298 | 302 | PF01048 | 0.424 |
MOD_GlcNHglycan | 386 | 389 | PF01048 | 0.439 |
MOD_GlcNHglycan | 414 | 417 | PF01048 | 0.519 |
MOD_GlcNHglycan | 42 | 45 | PF01048 | 0.460 |
MOD_GlcNHglycan | 532 | 535 | PF01048 | 0.724 |
MOD_GlcNHglycan | 537 | 540 | PF01048 | 0.667 |
MOD_GSK3_1 | 160 | 167 | PF00069 | 0.516 |
MOD_GSK3_1 | 182 | 189 | PF00069 | 0.389 |
MOD_GSK3_1 | 192 | 199 | PF00069 | 0.377 |
MOD_GSK3_1 | 287 | 294 | PF00069 | 0.388 |
MOD_GSK3_1 | 342 | 349 | PF00069 | 0.528 |
MOD_GSK3_1 | 361 | 368 | PF00069 | 0.231 |
MOD_GSK3_1 | 40 | 47 | PF00069 | 0.463 |
MOD_GSK3_1 | 400 | 407 | PF00069 | 0.594 |
MOD_GSK3_1 | 513 | 520 | PF00069 | 0.699 |
MOD_GSK3_1 | 67 | 74 | PF00069 | 0.507 |
MOD_N-GLC_1 | 103 | 108 | PF02516 | 0.389 |
MOD_N-GLC_1 | 192 | 197 | PF02516 | 0.538 |
MOD_NEK2_1 | 160 | 165 | PF00069 | 0.497 |
MOD_NEK2_1 | 184 | 189 | PF00069 | 0.479 |
MOD_NEK2_1 | 255 | 260 | PF00069 | 0.514 |
MOD_NEK2_1 | 328 | 333 | PF00069 | 0.431 |
MOD_NEK2_1 | 342 | 347 | PF00069 | 0.482 |
MOD_NEK2_1 | 348 | 353 | PF00069 | 0.526 |
MOD_NEK2_1 | 358 | 363 | PF00069 | 0.331 |
MOD_NEK2_1 | 400 | 405 | PF00069 | 0.605 |
MOD_NEK2_1 | 447 | 452 | PF00069 | 0.449 |
MOD_NEK2_1 | 495 | 500 | PF00069 | 0.365 |
MOD_NEK2_1 | 71 | 76 | PF00069 | 0.421 |
MOD_PIKK_1 | 202 | 208 | PF00454 | 0.504 |
MOD_PIKK_1 | 48 | 54 | PF00454 | 0.543 |
MOD_PIKK_1 | 71 | 77 | PF00454 | 0.416 |
MOD_PK_1 | 45 | 51 | PF00069 | 0.597 |
MOD_PKA_1 | 45 | 51 | PF00069 | 0.529 |
MOD_PKA_2 | 346 | 352 | PF00069 | 0.557 |
MOD_PKA_2 | 44 | 50 | PF00069 | 0.474 |
MOD_Plk_1 | 447 | 453 | PF00069 | 0.429 |
MOD_Plk_4 | 204 | 210 | PF00069 | 0.354 |
MOD_Plk_4 | 287 | 293 | PF00069 | 0.362 |
MOD_Plk_4 | 348 | 354 | PF00069 | 0.516 |
MOD_Plk_4 | 361 | 367 | PF00069 | 0.501 |
MOD_Plk_4 | 447 | 453 | PF00069 | 0.406 |
MOD_ProDKin_1 | 21 | 27 | PF00069 | 0.490 |
MOD_ProDKin_1 | 270 | 276 | PF00069 | 0.368 |
MOD_ProDKin_1 | 291 | 297 | PF00069 | 0.354 |
MOD_ProDKin_1 | 317 | 323 | PF00069 | 0.443 |
MOD_ProDKin_1 | 423 | 429 | PF00069 | 0.476 |
MOD_ProDKin_1 | 525 | 531 | PF00069 | 0.669 |
MOD_SUMO_for_1 | 221 | 224 | PF00179 | 0.479 |
MOD_SUMO_rev_2 | 210 | 219 | PF00179 | 0.521 |
MOD_SUMO_rev_2 | 368 | 375 | PF00179 | 0.498 |
MOD_SUMO_rev_2 | 56 | 61 | PF00179 | 0.504 |
TRG_DiLeu_BaLyEn_6 | 234 | 239 | PF01217 | 0.295 |
TRG_ENDOCYTIC_2 | 251 | 254 | PF00928 | 0.360 |
TRG_ENDOCYTIC_2 | 81 | 84 | PF00928 | 0.419 |
TRG_ER_diArg_1 | 147 | 149 | PF00400 | 0.447 |
TRG_ER_diArg_1 | 504 | 506 | PF00400 | 0.537 |
TRG_Pf-PMV_PEXEL_1 | 237 | 241 | PF00026 | 0.466 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P620 | Leptomonas seymouri | 72% | 100% |
A0A0S4J1E1 | Bodo saltans | 33% | 97% |
A0A1X0NY27 | Trypanosomatidae | 39% | 100% |
A0A3R7RTJ3 | Trypanosoma rangeli | 38% | 100% |
A0A3S7WZE8 | Leishmania donovani | 95% | 100% |
A4HED4 | Leishmania braziliensis | 86% | 100% |
A4I1T1 | Leishmania infantum | 95% | 100% |
E9AXW5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
V5B817 | Trypanosoma cruzi | 40% | 100% |