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: Q4QBY9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 14 | 18 | PF00656 | 0.706 |
CLV_C14_Caspase3-7 | 407 | 411 | PF00656 | 0.740 |
CLV_NRD_NRD_1 | 138 | 140 | PF00675 | 0.459 |
CLV_NRD_NRD_1 | 261 | 263 | PF00675 | 0.628 |
CLV_NRD_NRD_1 | 271 | 273 | PF00675 | 0.586 |
CLV_NRD_NRD_1 | 311 | 313 | PF00675 | 0.479 |
CLV_NRD_NRD_1 | 336 | 338 | PF00675 | 0.614 |
CLV_NRD_NRD_1 | 420 | 422 | PF00675 | 0.680 |
CLV_PCSK_FUR_1 | 418 | 422 | PF00082 | 0.710 |
CLV_PCSK_KEX2_1 | 140 | 142 | PF00082 | 0.532 |
CLV_PCSK_KEX2_1 | 205 | 207 | PF00082 | 0.473 |
CLV_PCSK_KEX2_1 | 216 | 218 | PF00082 | 0.582 |
CLV_PCSK_KEX2_1 | 231 | 233 | PF00082 | 0.606 |
CLV_PCSK_KEX2_1 | 261 | 263 | PF00082 | 0.604 |
CLV_PCSK_KEX2_1 | 311 | 313 | PF00082 | 0.479 |
CLV_PCSK_KEX2_1 | 336 | 338 | PF00082 | 0.614 |
CLV_PCSK_KEX2_1 | 354 | 356 | PF00082 | 0.637 |
CLV_PCSK_KEX2_1 | 420 | 422 | PF00082 | 0.754 |
CLV_PCSK_PC1ET2_1 | 140 | 142 | PF00082 | 0.379 |
CLV_PCSK_PC1ET2_1 | 205 | 207 | PF00082 | 0.521 |
CLV_PCSK_PC1ET2_1 | 216 | 218 | PF00082 | 0.467 |
CLV_PCSK_PC1ET2_1 | 231 | 233 | PF00082 | 0.623 |
CLV_PCSK_PC1ET2_1 | 354 | 356 | PF00082 | 0.679 |
CLV_PCSK_SKI1_1 | 420 | 424 | PF00082 | 0.786 |
CLV_PCSK_SKI1_1 | 434 | 438 | PF00082 | 0.629 |
CLV_PCSK_SKI1_1 | 456 | 460 | PF00082 | 0.612 |
CLV_PCSK_SKI1_1 | 73 | 77 | PF00082 | 0.596 |
CLV_Separin_Metazoa | 165 | 169 | PF03568 | 0.494 |
CLV_Separin_Metazoa | 253 | 257 | PF03568 | 0.618 |
DEG_APCC_DBOX_1 | 121 | 129 | PF00400 | 0.549 |
DEG_APCC_DBOX_1 | 402 | 410 | PF00400 | 0.724 |
DEG_COP1_1 | 17 | 26 | PF00400 | 0.644 |
DEG_SPOP_SBC_1 | 5 | 9 | PF00917 | 0.744 |
DOC_MAPK_gen_1 | 278 | 285 | PF00069 | 0.574 |
DOC_PP2B_LxvP_1 | 466 | 469 | PF13499 | 0.539 |
DOC_PP4_MxPP_1 | 1 | 4 | PF00568 | 0.774 |
DOC_USP7_MATH_1 | 113 | 117 | PF00917 | 0.473 |
DOC_USP7_MATH_1 | 37 | 41 | PF00917 | 0.631 |
DOC_USP7_MATH_1 | 428 | 432 | PF00917 | 0.676 |
DOC_USP7_MATH_1 | 5 | 9 | PF00917 | 0.552 |
DOC_WW_Pin1_4 | 15 | 20 | PF00397 | 0.737 |
DOC_WW_Pin1_4 | 426 | 431 | PF00397 | 0.679 |
LIG_14-3-3_CanoR_1 | 122 | 130 | PF00244 | 0.596 |
LIG_14-3-3_CanoR_1 | 171 | 175 | PF00244 | 0.566 |
LIG_14-3-3_CanoR_1 | 29 | 34 | PF00244 | 0.673 |
LIG_14-3-3_CanoR_1 | 420 | 427 | PF00244 | 0.670 |
LIG_14-3-3_CanoR_1 | 456 | 466 | PF00244 | 0.711 |
LIG_14-3-3_CanoR_1 | 73 | 78 | PF00244 | 0.658 |
LIG_Actin_WH2_2 | 222 | 239 | PF00022 | 0.572 |
LIG_Actin_WH2_2 | 331 | 348 | PF00022 | 0.606 |
LIG_Actin_WH2_2 | 79 | 96 | PF00022 | 0.607 |
LIG_BRCT_BRCA1_1 | 158 | 162 | PF00533 | 0.534 |
LIG_BRCT_BRCA1_1 | 367 | 371 | PF00533 | 0.588 |
LIG_Clathr_ClatBox_1 | 111 | 115 | PF01394 | 0.496 |
LIG_deltaCOP1_diTrp_1 | 27 | 33 | PF00928 | 0.669 |
LIG_DLG_GKlike_1 | 217 | 225 | PF00625 | 0.572 |
LIG_EH1_1 | 105 | 113 | PF00400 | 0.620 |
LIG_FHA_1 | 118 | 124 | PF00498 | 0.514 |
LIG_FHA_1 | 151 | 157 | PF00498 | 0.503 |
LIG_FHA_1 | 18 | 24 | PF00498 | 0.762 |
LIG_FHA_1 | 98 | 104 | PF00498 | 0.402 |
LIG_FHA_2 | 302 | 308 | PF00498 | 0.588 |
LIG_FHA_2 | 9 | 15 | PF00498 | 0.735 |
LIG_LIR_Gen_1 | 250 | 257 | PF02991 | 0.562 |
LIG_LIR_Gen_1 | 27 | 37 | PF02991 | 0.590 |
LIG_LIR_Gen_1 | 279 | 289 | PF02991 | 0.515 |
LIG_LIR_Nem_3 | 190 | 195 | PF02991 | 0.523 |
LIG_LIR_Nem_3 | 250 | 254 | PF02991 | 0.553 |
LIG_LIR_Nem_3 | 27 | 33 | PF02991 | 0.571 |
LIG_LIR_Nem_3 | 279 | 285 | PF02991 | 0.520 |
LIG_SH2_GRB2like | 189 | 192 | PF00017 | 0.414 |
LIG_SH2_NCK_1 | 425 | 429 | PF00017 | 0.693 |
LIG_SH2_SRC | 68 | 71 | PF00017 | 0.624 |
LIG_SH2_STAP1 | 203 | 207 | PF00017 | 0.564 |
LIG_SH2_STAP1 | 251 | 255 | PF00017 | 0.623 |
LIG_SUMO_SIM_par_1 | 109 | 117 | PF11976 | 0.572 |
LIG_TRAF2_1 | 12 | 15 | PF00917 | 0.751 |
LIG_TRAF2_1 | 239 | 242 | PF00917 | 0.628 |
LIG_TRAF2_1 | 25 | 28 | PF00917 | 0.532 |
LIG_TRAF2_1 | 300 | 303 | PF00917 | 0.587 |
LIG_TRAF2_1 | 328 | 331 | PF00917 | 0.503 |
LIG_TRAF2_1 | 460 | 463 | PF00917 | 0.674 |
LIG_TRAF2_1 | 67 | 70 | PF00917 | 0.628 |
MOD_CK1_1 | 40 | 46 | PF00069 | 0.589 |
MOD_CK1_1 | 457 | 463 | PF00069 | 0.645 |
MOD_CK1_1 | 48 | 54 | PF00069 | 0.597 |
MOD_CK1_1 | 8 | 14 | PF00069 | 0.599 |
MOD_CK2_1 | 187 | 193 | PF00069 | 0.587 |
MOD_CK2_1 | 22 | 28 | PF00069 | 0.616 |
MOD_CK2_1 | 236 | 242 | PF00069 | 0.624 |
MOD_CK2_1 | 43 | 49 | PF00069 | 0.662 |
MOD_CK2_1 | 457 | 463 | PF00069 | 0.649 |
MOD_CK2_1 | 8 | 14 | PF00069 | 0.738 |
MOD_CK2_1 | 96 | 102 | PF00069 | 0.433 |
MOD_GlcNHglycan | 406 | 409 | PF01048 | 0.710 |
MOD_GlcNHglycan | 456 | 459 | PF01048 | 0.665 |
MOD_GSK3_1 | 113 | 120 | PF00069 | 0.315 |
MOD_GSK3_1 | 15 | 22 | PF00069 | 0.653 |
MOD_GSK3_1 | 166 | 173 | PF00069 | 0.533 |
MOD_GSK3_1 | 187 | 194 | PF00069 | 0.604 |
MOD_GSK3_1 | 236 | 243 | PF00069 | 0.555 |
MOD_GSK3_1 | 4 | 11 | PF00069 | 0.727 |
MOD_GSK3_1 | 93 | 100 | PF00069 | 0.455 |
MOD_NEK2_1 | 118 | 123 | PF00069 | 0.550 |
MOD_NEK2_1 | 156 | 161 | PF00069 | 0.547 |
MOD_NEK2_1 | 170 | 175 | PF00069 | 0.450 |
MOD_NEK2_1 | 225 | 230 | PF00069 | 0.540 |
MOD_NEK2_1 | 6 | 11 | PF00069 | 0.769 |
MOD_PIKK_1 | 68 | 74 | PF00454 | 0.621 |
MOD_PKA_1 | 420 | 426 | PF00069 | 0.742 |
MOD_PKA_2 | 170 | 176 | PF00069 | 0.527 |
MOD_PKA_2 | 28 | 34 | PF00069 | 0.671 |
MOD_PKA_2 | 404 | 410 | PF00069 | 0.719 |
MOD_PKA_2 | 420 | 426 | PF00069 | 0.742 |
MOD_PKA_2 | 93 | 99 | PF00069 | 0.602 |
MOD_PKB_1 | 299 | 307 | PF00069 | 0.640 |
MOD_PKB_1 | 418 | 426 | PF00069 | 0.704 |
MOD_PKB_1 | 447 | 455 | PF00069 | 0.655 |
MOD_Plk_1 | 301 | 307 | PF00069 | 0.614 |
MOD_Plk_1 | 40 | 46 | PF00069 | 0.604 |
MOD_Plk_4 | 301 | 307 | PF00069 | 0.620 |
MOD_ProDKin_1 | 15 | 21 | PF00069 | 0.735 |
MOD_ProDKin_1 | 426 | 432 | PF00069 | 0.680 |
MOD_SUMO_for_1 | 230 | 233 | PF00179 | 0.612 |
MOD_SUMO_rev_2 | 137 | 142 | PF00179 | 0.375 |
TRG_DiLeu_BaEn_1 | 250 | 255 | PF01217 | 0.622 |
TRG_DiLeu_BaEn_4 | 137 | 143 | PF01217 | 0.610 |
TRG_ENDOCYTIC_2 | 189 | 192 | PF00928 | 0.492 |
TRG_ENDOCYTIC_2 | 251 | 254 | PF00928 | 0.587 |
TRG_ER_diArg_1 | 139 | 142 | PF00400 | 0.566 |
TRG_ER_diArg_1 | 298 | 301 | PF00400 | 0.590 |
TRG_ER_diArg_1 | 336 | 338 | PF00400 | 0.574 |
TRG_Pf-PMV_PEXEL_1 | 314 | 318 | PF00026 | 0.477 |
TRG_Pf-PMV_PEXEL_1 | 73 | 78 | PF00026 | 0.619 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1P9S5 | Leptomonas seymouri | 67% | 91% |
A0A1X0NTJ5 | Trypanosomatidae | 32% | 78% |
A0A3S7WWY1 | Leishmania donovani | 93% | 100% |
A0A422N4N0 | Trypanosoma rangeli | 35% | 75% |
A4HC57 | Leishmania braziliensis | 85% | 100% |
E9AGY5 | Leishmania infantum | 94% | 81% |
E9AVJ0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
V5BK97 | Trypanosoma cruzi | 36% | 100% |