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: A0A3Q8IRG7
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 216 | 218 | PF00675 | 0.371 |
CLV_NRD_NRD_1 | 431 | 433 | PF00675 | 0.603 |
CLV_NRD_NRD_1 | 6 | 8 | PF00675 | 0.593 |
CLV_PCSK_KEX2_1 | 216 | 218 | PF00082 | 0.380 |
CLV_PCSK_KEX2_1 | 404 | 406 | PF00082 | 0.673 |
CLV_PCSK_KEX2_1 | 431 | 433 | PF00082 | 0.699 |
CLV_PCSK_PC1ET2_1 | 404 | 406 | PF00082 | 0.673 |
CLV_PCSK_SKI1_1 | 194 | 198 | PF00082 | 0.407 |
CLV_PCSK_SKI1_1 | 333 | 337 | PF00082 | 0.592 |
CLV_PCSK_SKI1_1 | 376 | 380 | PF00082 | 0.710 |
DEG_APCC_DBOX_1 | 332 | 340 | PF00400 | 0.516 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.630 |
DEG_SPOP_SBC_1 | 100 | 104 | PF00917 | 0.512 |
DEG_SPOP_SBC_1 | 245 | 249 | PF00917 | 0.596 |
DOC_CKS1_1 | 23 | 28 | PF01111 | 0.551 |
DOC_MAPK_gen_1 | 7 | 15 | PF00069 | 0.593 |
DOC_MAPK_MEF2A_6 | 33 | 40 | PF00069 | 0.517 |
DOC_MAPK_MEF2A_6 | 8 | 17 | PF00069 | 0.493 |
DOC_PP4_FxxP_1 | 378 | 381 | PF00568 | 0.570 |
DOC_USP7_MATH_1 | 101 | 105 | PF00917 | 0.475 |
DOC_USP7_MATH_1 | 110 | 114 | PF00917 | 0.371 |
DOC_USP7_MATH_1 | 117 | 121 | PF00917 | 0.574 |
DOC_USP7_MATH_1 | 180 | 184 | PF00917 | 0.476 |
DOC_USP7_MATH_1 | 244 | 248 | PF00917 | 0.630 |
DOC_USP7_MATH_1 | 277 | 281 | PF00917 | 0.588 |
DOC_USP7_MATH_1 | 29 | 33 | PF00917 | 0.530 |
DOC_USP7_MATH_1 | 306 | 310 | PF00917 | 0.650 |
DOC_USP7_MATH_1 | 314 | 318 | PF00917 | 0.676 |
DOC_USP7_MATH_1 | 437 | 441 | PF00917 | 0.627 |
DOC_USP7_MATH_1 | 84 | 88 | PF00917 | 0.529 |
DOC_USP7_MATH_1 | 96 | 100 | PF00917 | 0.467 |
DOC_USP7_UBL2_3 | 380 | 384 | PF12436 | 0.638 |
DOC_WW_Pin1_4 | 22 | 27 | PF00397 | 0.533 |
DOC_WW_Pin1_4 | 258 | 263 | PF00397 | 0.496 |
DOC_WW_Pin1_4 | 321 | 326 | PF00397 | 0.600 |
DOC_WW_Pin1_4 | 342 | 347 | PF00397 | 0.626 |
LIG_14-3-3_CanoR_1 | 124 | 129 | PF00244 | 0.494 |
LIG_14-3-3_CanoR_1 | 278 | 284 | PF00244 | 0.639 |
LIG_14-3-3_CanoR_1 | 330 | 336 | PF00244 | 0.521 |
LIG_BIR_III_4 | 243 | 247 | PF00653 | 0.546 |
LIG_BRCT_BRCA1_1 | 13 | 17 | PF00533 | 0.593 |
LIG_CtBP_PxDLS_1 | 443 | 447 | PF00389 | 0.484 |
LIG_deltaCOP1_diTrp_1 | 202 | 210 | PF00928 | 0.481 |
LIG_deltaCOP1_diTrp_1 | 9 | 18 | PF00928 | 0.444 |
LIG_FHA_1 | 106 | 112 | PF00498 | 0.677 |
LIG_FHA_1 | 247 | 253 | PF00498 | 0.519 |
LIG_FHA_1 | 274 | 280 | PF00498 | 0.615 |
LIG_FHA_1 | 287 | 293 | PF00498 | 0.652 |
LIG_FHA_1 | 398 | 404 | PF00498 | 0.636 |
LIG_FHA_1 | 408 | 414 | PF00498 | 0.417 |
LIG_FHA_1 | 45 | 51 | PF00498 | 0.449 |
LIG_LIR_Gen_1 | 136 | 146 | PF02991 | 0.345 |
LIG_LIR_Gen_1 | 66 | 76 | PF02991 | 0.388 |
LIG_LIR_Gen_1 | 81 | 90 | PF02991 | 0.386 |
LIG_LIR_Nem_3 | 136 | 141 | PF02991 | 0.347 |
LIG_LIR_Nem_3 | 191 | 196 | PF02991 | 0.448 |
LIG_LIR_Nem_3 | 66 | 72 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 81 | 86 | PF02991 | 0.392 |
LIG_PDZ_Class_1 | 442 | 447 | PF00595 | 0.599 |
LIG_PTB_Apo_2 | 334 | 341 | PF02174 | 0.592 |
LIG_SH2_CRK | 350 | 354 | PF00017 | 0.406 |
LIG_SH2_NCK_1 | 28 | 32 | PF00017 | 0.614 |
LIG_SH2_PTP2 | 174 | 177 | PF00017 | 0.384 |
LIG_SH2_SRC | 174 | 177 | PF00017 | 0.384 |
LIG_SH2_STAP1 | 374 | 378 | PF00017 | 0.611 |
LIG_SH2_STAT5 | 138 | 141 | PF00017 | 0.333 |
LIG_SH2_STAT5 | 174 | 177 | PF00017 | 0.449 |
LIG_SH2_STAT5 | 221 | 224 | PF00017 | 0.470 |
LIG_SH3_1 | 39 | 45 | PF00018 | 0.491 |
LIG_SH3_3 | 174 | 180 | PF00018 | 0.526 |
LIG_SH3_3 | 256 | 262 | PF00018 | 0.504 |
LIG_SH3_3 | 319 | 325 | PF00018 | 0.598 |
LIG_SH3_3 | 39 | 45 | PF00018 | 0.479 |
LIG_SH3_4 | 380 | 387 | PF00018 | 0.562 |
LIG_SUMO_SIM_anti_2 | 412 | 418 | PF11976 | 0.651 |
LIG_SUMO_SIM_par_1 | 410 | 418 | PF11976 | 0.653 |
LIG_WRC_WIRS_1 | 315 | 320 | PF05994 | 0.705 |
LIG_WRC_WIRS_1 | 332 | 337 | PF05994 | 0.386 |
LIG_WW_3 | 340 | 344 | PF00397 | 0.595 |
MOD_CDK_SPxxK_3 | 342 | 349 | PF00069 | 0.624 |
MOD_CK1_1 | 324 | 330 | PF00069 | 0.509 |
MOD_CK1_1 | 99 | 105 | PF00069 | 0.609 |
MOD_CK2_1 | 60 | 66 | PF00069 | 0.378 |
MOD_GlcNHglycan | 103 | 106 | PF01048 | 0.611 |
MOD_GlcNHglycan | 119 | 122 | PF01048 | 0.547 |
MOD_GlcNHglycan | 256 | 259 | PF01048 | 0.700 |
MOD_GlcNHglycan | 279 | 282 | PF01048 | 0.568 |
MOD_GlcNHglycan | 294 | 297 | PF01048 | 0.682 |
MOD_GlcNHglycan | 308 | 311 | PF01048 | 0.491 |
MOD_GlcNHglycan | 391 | 394 | PF01048 | 0.585 |
MOD_GlcNHglycan | 66 | 69 | PF01048 | 0.414 |
MOD_GlcNHglycan | 98 | 101 | PF01048 | 0.578 |
MOD_GSK3_1 | 105 | 112 | PF00069 | 0.552 |
MOD_GSK3_1 | 18 | 25 | PF00069 | 0.493 |
MOD_GSK3_1 | 205 | 212 | PF00069 | 0.424 |
MOD_GSK3_1 | 254 | 261 | PF00069 | 0.619 |
MOD_GSK3_1 | 273 | 280 | PF00069 | 0.573 |
MOD_GSK3_1 | 324 | 331 | PF00069 | 0.561 |
MOD_GSK3_1 | 60 | 67 | PF00069 | 0.546 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.416 |
MOD_GSK3_1 | 96 | 103 | PF00069 | 0.524 |
MOD_NEK2_1 | 18 | 23 | PF00069 | 0.528 |
MOD_NEK2_1 | 200 | 205 | PF00069 | 0.374 |
MOD_NEK2_1 | 206 | 211 | PF00069 | 0.442 |
MOD_NEK2_1 | 292 | 297 | PF00069 | 0.662 |
MOD_NEK2_1 | 335 | 340 | PF00069 | 0.588 |
MOD_PIKK_1 | 2 | 8 | PF00454 | 0.602 |
MOD_PIKK_1 | 44 | 50 | PF00454 | 0.463 |
MOD_PKA_2 | 117 | 123 | PF00069 | 0.558 |
MOD_PKA_2 | 277 | 283 | PF00069 | 0.646 |
MOD_PKA_2 | 91 | 97 | PF00069 | 0.472 |
MOD_PKB_1 | 22 | 30 | PF00069 | 0.531 |
MOD_Plk_1 | 328 | 334 | PF00069 | 0.606 |
MOD_Plk_2-3 | 60 | 66 | PF00069 | 0.378 |
MOD_Plk_4 | 110 | 116 | PF00069 | 0.517 |
MOD_Plk_4 | 180 | 186 | PF00069 | 0.506 |
MOD_Plk_4 | 200 | 206 | PF00069 | 0.471 |
MOD_Plk_4 | 335 | 341 | PF00069 | 0.545 |
MOD_Plk_4 | 60 | 66 | PF00069 | 0.499 |
MOD_ProDKin_1 | 22 | 28 | PF00069 | 0.541 |
MOD_ProDKin_1 | 258 | 264 | PF00069 | 0.490 |
MOD_ProDKin_1 | 321 | 327 | PF00069 | 0.595 |
MOD_ProDKin_1 | 342 | 348 | PF00069 | 0.622 |
MOD_SUMO_for_1 | 379 | 382 | PF00179 | 0.564 |
MOD_SUMO_for_1 | 403 | 406 | PF00179 | 0.705 |
MOD_SUMO_rev_2 | 231 | 240 | PF00179 | 0.600 |
TRG_DiLeu_BaEn_1 | 166 | 171 | PF01217 | 0.307 |
TRG_ENDOCYTIC_2 | 138 | 141 | PF00928 | 0.345 |
TRG_ENDOCYTIC_2 | 174 | 177 | PF00928 | 0.464 |
TRG_ENDOCYTIC_2 | 193 | 196 | PF00928 | 0.469 |
TRG_ER_diArg_1 | 216 | 218 | PF00400 | 0.372 |
TRG_ER_diArg_1 | 430 | 432 | PF00400 | 0.641 |
TRG_Pf-PMV_PEXEL_1 | 216 | 220 | PF00026 | 0.413 |
TRG_Pf-PMV_PEXEL_1 | 431 | 435 | PF00026 | 0.732 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2Q6 | Leptomonas seymouri | 65% | 95% |
A0A0S4KK06 | Bodo saltans | 26% | 92% |
A0A1X0NJ10 | Trypanosomatidae | 32% | 100% |
A0A3R7NSU2 | Trypanosoma rangeli | 33% | 100% |
A4HHJ0 | Leishmania braziliensis | 87% | 100% |
A4I4P8 | Leishmania infantum | 100% | 100% |
C9ZN48 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
E9AE51 | Leishmania major | 95% | 100% |
E9ALN4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |
V5BIJ5 | Trypanosoma cruzi | 32% | 100% |