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: Q4Q0I0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 110 | 114 | PF00656 | 0.515 |
CLV_C14_Caspase3-7 | 23 | 27 | PF00656 | 0.585 |
CLV_C14_Caspase3-7 | 333 | 337 | PF00656 | 0.471 |
CLV_C14_Caspase3-7 | 392 | 396 | PF00656 | 0.577 |
CLV_C14_Caspase3-7 | 45 | 49 | PF00656 | 0.513 |
CLV_NRD_NRD_1 | 169 | 171 | PF00675 | 0.567 |
CLV_NRD_NRD_1 | 274 | 276 | PF00675 | 0.472 |
CLV_NRD_NRD_1 | 31 | 33 | PF00675 | 0.595 |
CLV_NRD_NRD_1 | 386 | 388 | PF00675 | 0.637 |
CLV_PCSK_FUR_1 | 384 | 388 | PF00082 | 0.607 |
CLV_PCSK_KEX2_1 | 274 | 276 | PF00082 | 0.509 |
CLV_PCSK_KEX2_1 | 282 | 284 | PF00082 | 0.634 |
CLV_PCSK_KEX2_1 | 386 | 388 | PF00082 | 0.639 |
CLV_PCSK_PC1ET2_1 | 282 | 284 | PF00082 | 0.654 |
CLV_PCSK_PC1ET2_1 | 386 | 388 | PF00082 | 0.639 |
CLV_PCSK_PC7_1 | 384 | 390 | PF00082 | 0.657 |
CLV_PCSK_SKI1_1 | 267 | 271 | PF00082 | 0.506 |
CLV_PCSK_SKI1_1 | 305 | 309 | PF00082 | 0.487 |
DEG_APCC_DBOX_1 | 177 | 185 | PF00400 | 0.448 |
DEG_APCC_DBOX_1 | 266 | 274 | PF00400 | 0.535 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.463 |
DOC_CKS1_1 | 200 | 205 | PF01111 | 0.515 |
DOC_CYCLIN_RxL_1 | 264 | 271 | PF00134 | 0.473 |
DOC_MAPK_gen_1 | 142 | 149 | PF00069 | 0.530 |
DOC_MAPK_MEF2A_6 | 316 | 325 | PF00069 | 0.456 |
DOC_MAPK_MEF2A_6 | 358 | 366 | PF00069 | 0.468 |
DOC_PP2B_LxvP_1 | 122 | 125 | PF13499 | 0.520 |
DOC_PP2B_LxvP_1 | 261 | 264 | PF13499 | 0.536 |
DOC_PP2B_LxvP_1 | 345 | 348 | PF13499 | 0.499 |
DOC_USP7_MATH_1 | 136 | 140 | PF00917 | 0.556 |
DOC_USP7_MATH_1 | 51 | 55 | PF00917 | 0.616 |
DOC_WW_Pin1_4 | 199 | 204 | PF00397 | 0.669 |
DOC_WW_Pin1_4 | 33 | 38 | PF00397 | 0.678 |
LIG_14-3-3_CanoR_1 | 146 | 155 | PF00244 | 0.494 |
LIG_14-3-3_CanoR_1 | 216 | 226 | PF00244 | 0.602 |
LIG_14-3-3_CanoR_1 | 258 | 264 | PF00244 | 0.429 |
LIG_14-3-3_CanoR_1 | 296 | 304 | PF00244 | 0.435 |
LIG_14-3-3_CanoR_1 | 316 | 322 | PF00244 | 0.462 |
LIG_14-3-3_CanoR_1 | 67 | 75 | PF00244 | 0.368 |
LIG_14-3-3_CanoR_1 | 92 | 96 | PF00244 | 0.547 |
LIG_Actin_WH2_2 | 406 | 424 | PF00022 | 0.448 |
LIG_BIR_III_2 | 48 | 52 | PF00653 | 0.468 |
LIG_FHA_1 | 195 | 201 | PF00498 | 0.586 |
LIG_FHA_1 | 70 | 76 | PF00498 | 0.400 |
LIG_FHA_2 | 238 | 244 | PF00498 | 0.679 |
LIG_FHA_2 | 403 | 409 | PF00498 | 0.578 |
LIG_FHA_2 | 72 | 78 | PF00498 | 0.549 |
LIG_LIR_Gen_1 | 299 | 308 | PF02991 | 0.452 |
LIG_LIR_Gen_1 | 66 | 75 | PF02991 | 0.536 |
LIG_LIR_Nem_3 | 188 | 193 | PF02991 | 0.568 |
LIG_LIR_Nem_3 | 299 | 304 | PF02991 | 0.442 |
LIG_LIR_Nem_3 | 66 | 71 | PF02991 | 0.518 |
LIG_LYPXL_SIV_4 | 300 | 308 | PF13949 | 0.465 |
LIG_NBox_RRM_1 | 331 | 341 | PF00076 | 0.441 |
LIG_NRBOX | 265 | 271 | PF00104 | 0.535 |
LIG_NRBOX | 340 | 346 | PF00104 | 0.470 |
LIG_SH2_CRK | 17 | 21 | PF00017 | 0.608 |
LIG_SH2_STAP1 | 190 | 194 | PF00017 | 0.544 |
LIG_SH2_STAT5 | 148 | 151 | PF00017 | 0.518 |
LIG_SH2_STAT5 | 193 | 196 | PF00017 | 0.582 |
LIG_SH2_STAT5 | 2 | 5 | PF00017 | 0.517 |
LIG_SH3_3 | 197 | 203 | PF00018 | 0.489 |
LIG_SH3_3 | 224 | 230 | PF00018 | 0.665 |
LIG_SH3_3 | 31 | 37 | PF00018 | 0.603 |
LIG_SH3_3 | 361 | 367 | PF00018 | 0.660 |
LIG_SUMO_SIM_par_1 | 152 | 159 | PF11976 | 0.456 |
LIG_SUMO_SIM_par_1 | 2 | 8 | PF11976 | 0.508 |
LIG_TRAF2_1 | 156 | 159 | PF00917 | 0.544 |
LIG_TYR_ITIM | 15 | 20 | PF00017 | 0.595 |
MOD_CK1_1 | 114 | 120 | PF00069 | 0.796 |
MOD_CK1_1 | 201 | 207 | PF00069 | 0.671 |
MOD_CK1_1 | 217 | 223 | PF00069 | 0.646 |
MOD_CK1_1 | 350 | 356 | PF00069 | 0.431 |
MOD_CK1_1 | 69 | 75 | PF00069 | 0.368 |
MOD_CK2_1 | 153 | 159 | PF00069 | 0.423 |
MOD_CK2_1 | 2 | 8 | PF00069 | 0.508 |
MOD_CK2_1 | 237 | 243 | PF00069 | 0.643 |
MOD_CK2_1 | 296 | 302 | PF00069 | 0.460 |
MOD_CK2_1 | 402 | 408 | PF00069 | 0.612 |
MOD_Cter_Amidation | 384 | 387 | PF01082 | 0.647 |
MOD_GlcNHglycan | 100 | 103 | PF01048 | 0.599 |
MOD_GlcNHglycan | 113 | 116 | PF01048 | 0.631 |
MOD_GlcNHglycan | 138 | 141 | PF01048 | 0.606 |
MOD_GlcNHglycan | 23 | 26 | PF01048 | 0.739 |
MOD_GlcNHglycan | 253 | 256 | PF01048 | 0.473 |
MOD_GlcNHglycan | 261 | 264 | PF01048 | 0.475 |
MOD_GlcNHglycan | 298 | 301 | PF01048 | 0.495 |
MOD_GlcNHglycan | 349 | 352 | PF01048 | 0.359 |
MOD_GlcNHglycan | 367 | 370 | PF01048 | 0.688 |
MOD_GlcNHglycan | 431 | 434 | PF01048 | 0.374 |
MOD_GlcNHglycan | 44 | 47 | PF01048 | 0.720 |
MOD_GSK3_1 | 114 | 121 | PF00069 | 0.615 |
MOD_GSK3_1 | 149 | 156 | PF00069 | 0.546 |
MOD_GSK3_1 | 194 | 201 | PF00069 | 0.590 |
MOD_GSK3_1 | 217 | 224 | PF00069 | 0.636 |
MOD_GSK3_1 | 232 | 239 | PF00069 | 0.716 |
MOD_GSK3_1 | 402 | 409 | PF00069 | 0.648 |
MOD_NEK2_1 | 147 | 152 | PF00069 | 0.505 |
MOD_NEK2_1 | 257 | 262 | PF00069 | 0.439 |
MOD_NEK2_1 | 352 | 357 | PF00069 | 0.562 |
MOD_NEK2_1 | 428 | 433 | PF00069 | 0.457 |
MOD_PIKK_1 | 268 | 274 | PF00454 | 0.565 |
MOD_PIKK_1 | 400 | 406 | PF00454 | 0.684 |
MOD_PKA_1 | 170 | 176 | PF00069 | 0.568 |
MOD_PKA_2 | 257 | 263 | PF00069 | 0.440 |
MOD_PKA_2 | 28 | 34 | PF00069 | 0.788 |
MOD_PKA_2 | 429 | 435 | PF00069 | 0.411 |
MOD_PKA_2 | 66 | 72 | PF00069 | 0.435 |
MOD_PKA_2 | 91 | 97 | PF00069 | 0.537 |
MOD_Plk_1 | 185 | 191 | PF00069 | 0.440 |
MOD_Plk_1 | 326 | 332 | PF00069 | 0.523 |
MOD_Plk_4 | 2 | 8 | PF00069 | 0.430 |
MOD_Plk_4 | 352 | 358 | PF00069 | 0.480 |
MOD_ProDKin_1 | 199 | 205 | PF00069 | 0.669 |
MOD_ProDKin_1 | 33 | 39 | PF00069 | 0.674 |
MOD_SUMO_rev_2 | 368 | 376 | PF00179 | 0.692 |
TRG_DiLeu_BaEn_1 | 419 | 424 | PF01217 | 0.481 |
TRG_DiLeu_BaLyEn_6 | 340 | 345 | PF01217 | 0.491 |
TRG_DiLeu_LyEn_5 | 419 | 424 | PF01217 | 0.336 |
TRG_ENDOCYTIC_2 | 17 | 20 | PF00928 | 0.605 |
TRG_ENDOCYTIC_2 | 301 | 304 | PF00928 | 0.438 |
TRG_ENDOCYTIC_2 | 68 | 71 | PF00928 | 0.424 |
TRG_ER_diArg_1 | 143 | 146 | PF00400 | 0.440 |
TRG_ER_diArg_1 | 273 | 275 | PF00400 | 0.497 |
TRG_Pf-PMV_PEXEL_1 | 267 | 272 | PF00026 | 0.611 |
TRG_Pf-PMV_PEXEL_1 | 291 | 295 | PF00026 | 0.470 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PEF3 | Leptomonas seymouri | 44% | 84% |
A0A1X0NLI7 | Trypanosomatidae | 29% | 100% |
A0A3Q8IPS4 | Leishmania donovani | 89% | 100% |
A0A3R7NLX1 | Trypanosoma rangeli | 28% | 100% |
A4HQ97 | Leishmania braziliensis | 69% | 100% |
D0A414 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
E9AHY4 | Leishmania infantum | 89% | 100% |
E9AU15 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |