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: 19 |
NetGPI | no | yes: 0, no: 19 |
Related structures:
AlphaFold database: E9AVU4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 106 | 110 | PF00656 | 0.633 |
CLV_C14_Caspase3-7 | 150 | 154 | PF00656 | 0.302 |
CLV_NRD_NRD_1 | 275 | 277 | PF00675 | 0.367 |
CLV_NRD_NRD_1 | 74 | 76 | PF00675 | 0.506 |
CLV_PCSK_KEX2_1 | 275 | 277 | PF00082 | 0.368 |
CLV_PCSK_KEX2_1 | 74 | 76 | PF00082 | 0.500 |
CLV_PCSK_SKI1_1 | 414 | 418 | PF00082 | 0.437 |
DEG_APCC_DBOX_1 | 73 | 81 | PF00400 | 0.577 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.568 |
DEG_SPOP_SBC_1 | 113 | 117 | PF00917 | 0.501 |
DOC_CKS1_1 | 236 | 241 | PF01111 | 0.378 |
DOC_MAPK_DCC_7 | 74 | 82 | PF00069 | 0.415 |
DOC_MAPK_gen_1 | 275 | 282 | PF00069 | 0.343 |
DOC_MAPK_gen_1 | 289 | 297 | PF00069 | 0.448 |
DOC_MAPK_gen_1 | 74 | 82 | PF00069 | 0.493 |
DOC_MAPK_MEF2A_6 | 289 | 297 | PF00069 | 0.511 |
DOC_MAPK_MEF2A_6 | 63 | 72 | PF00069 | 0.362 |
DOC_MAPK_MEF2A_6 | 74 | 82 | PF00069 | 0.481 |
DOC_MAPK_NFAT4_5 | 63 | 71 | PF00069 | 0.332 |
DOC_USP7_MATH_1 | 121 | 125 | PF00917 | 0.755 |
DOC_USP7_MATH_1 | 338 | 342 | PF00917 | 0.449 |
DOC_USP7_MATH_1 | 367 | 371 | PF00917 | 0.473 |
DOC_USP7_MATH_1 | 437 | 441 | PF00917 | 0.367 |
DOC_USP7_MATH_1 | 55 | 59 | PF00917 | 0.563 |
DOC_USP7_UBL2_3 | 216 | 220 | PF12436 | 0.283 |
DOC_WW_Pin1_4 | 208 | 213 | PF00397 | 0.429 |
DOC_WW_Pin1_4 | 235 | 240 | PF00397 | 0.550 |
DOC_WW_Pin1_4 | 386 | 391 | PF00397 | 0.470 |
DOC_WW_Pin1_4 | 392 | 397 | PF00397 | 0.528 |
DOC_WW_Pin1_4 | 87 | 92 | PF00397 | 0.656 |
LIG_14-3-3_CanoR_1 | 227 | 231 | PF00244 | 0.329 |
LIG_14-3-3_CanoR_1 | 275 | 283 | PF00244 | 0.359 |
LIG_14-3-3_CanoR_1 | 63 | 69 | PF00244 | 0.383 |
LIG_Actin_WH2_2 | 435 | 450 | PF00022 | 0.485 |
LIG_BIR_III_4 | 109 | 113 | PF00653 | 0.476 |
LIG_BRCT_BRCA1_1 | 369 | 373 | PF00533 | 0.466 |
LIG_Clathr_ClatBox_1 | 282 | 286 | PF01394 | 0.474 |
LIG_Clathr_ClatBox_1 | 377 | 381 | PF01394 | 0.347 |
LIG_deltaCOP1_diTrp_1 | 199 | 205 | PF00928 | 0.425 |
LIG_FHA_1 | 114 | 120 | PF00498 | 0.698 |
LIG_FHA_1 | 135 | 141 | PF00498 | 0.316 |
LIG_FHA_1 | 167 | 173 | PF00498 | 0.425 |
LIG_FHA_1 | 429 | 435 | PF00498 | 0.360 |
LIG_FHA_2 | 148 | 154 | PF00498 | 0.261 |
LIG_FHA_2 | 236 | 242 | PF00498 | 0.446 |
LIG_FHA_2 | 276 | 282 | PF00498 | 0.353 |
LIG_FHA_2 | 81 | 87 | PF00498 | 0.614 |
LIG_LIR_Apic_2 | 208 | 212 | PF02991 | 0.408 |
LIG_LIR_Gen_1 | 266 | 274 | PF02991 | 0.429 |
LIG_LIR_Nem_3 | 153 | 158 | PF02991 | 0.301 |
LIG_LIR_Nem_3 | 266 | 272 | PF02991 | 0.497 |
LIG_LIR_Nem_3 | 312 | 318 | PF02991 | 0.365 |
LIG_SH2_CRK | 316 | 320 | PF00017 | 0.349 |
LIG_SH2_STAT5 | 134 | 137 | PF00017 | 0.511 |
LIG_SH2_STAT5 | 155 | 158 | PF00017 | 0.310 |
LIG_SH2_STAT5 | 209 | 212 | PF00017 | 0.275 |
LIG_SH2_STAT5 | 224 | 227 | PF00017 | 0.219 |
LIG_SH2_STAT5 | 326 | 329 | PF00017 | 0.413 |
LIG_SH2_STAT5 | 359 | 362 | PF00017 | 0.317 |
LIG_SH2_STAT5 | 399 | 402 | PF00017 | 0.356 |
LIG_SH3_1 | 75 | 81 | PF00018 | 0.373 |
LIG_SH3_3 | 14 | 20 | PF00018 | 0.411 |
LIG_SH3_3 | 461 | 467 | PF00018 | 0.302 |
LIG_SH3_3 | 51 | 57 | PF00018 | 0.491 |
LIG_SH3_3 | 75 | 81 | PF00018 | 0.571 |
LIG_SUMO_SIM_par_1 | 168 | 173 | PF11976 | 0.437 |
LIG_UBA3_1 | 404 | 412 | PF00899 | 0.313 |
LIG_WRC_WIRS_1 | 202 | 207 | PF05994 | 0.418 |
MOD_CDK_SPxxK_3 | 386 | 393 | PF00069 | 0.326 |
MOD_CK1_1 | 211 | 217 | PF00069 | 0.288 |
MOD_CK1_1 | 229 | 235 | PF00069 | 0.387 |
MOD_CK1_1 | 237 | 243 | PF00069 | 0.486 |
MOD_CK1_1 | 32 | 38 | PF00069 | 0.315 |
MOD_CK1_1 | 361 | 367 | PF00069 | 0.320 |
MOD_CK1_1 | 428 | 434 | PF00069 | 0.304 |
MOD_CK1_1 | 87 | 93 | PF00069 | 0.761 |
MOD_CK2_1 | 235 | 241 | PF00069 | 0.438 |
MOD_CK2_1 | 80 | 86 | PF00069 | 0.591 |
MOD_GlcNHglycan | 105 | 108 | PF01048 | 0.734 |
MOD_GlcNHglycan | 231 | 234 | PF01048 | 0.532 |
MOD_GlcNHglycan | 31 | 34 | PF01048 | 0.351 |
MOD_GlcNHglycan | 390 | 393 | PF01048 | 0.539 |
MOD_GlcNHglycan | 56 | 60 | PF01048 | 0.512 |
MOD_GSK3_1 | 166 | 173 | PF00069 | 0.417 |
MOD_GSK3_1 | 201 | 208 | PF00069 | 0.365 |
MOD_GSK3_1 | 210 | 217 | PF00069 | 0.332 |
MOD_GSK3_1 | 25 | 32 | PF00069 | 0.313 |
MOD_GSK3_1 | 300 | 307 | PF00069 | 0.632 |
MOD_GSK3_1 | 334 | 341 | PF00069 | 0.405 |
MOD_GSK3_1 | 388 | 395 | PF00069 | 0.489 |
MOD_GSK3_1 | 64 | 71 | PF00069 | 0.394 |
MOD_GSK3_1 | 80 | 87 | PF00069 | 0.603 |
MOD_N-GLC_1 | 1 | 6 | PF02516 | 0.376 |
MOD_N-GLC_1 | 103 | 108 | PF02516 | 0.680 |
MOD_N-GLC_1 | 64 | 69 | PF02516 | 0.370 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.477 |
MOD_NEK2_1 | 170 | 175 | PF00069 | 0.420 |
MOD_NEK2_1 | 25 | 30 | PF00069 | 0.412 |
MOD_NEK2_1 | 425 | 430 | PF00069 | 0.277 |
MOD_NEK2_1 | 68 | 73 | PF00069 | 0.380 |
MOD_NEK2_2 | 121 | 126 | PF00069 | 0.548 |
MOD_NEK2_2 | 147 | 152 | PF00069 | 0.289 |
MOD_PIKK_1 | 11 | 17 | PF00454 | 0.418 |
MOD_PIKK_1 | 338 | 344 | PF00454 | 0.584 |
MOD_PKA_1 | 275 | 281 | PF00069 | 0.387 |
MOD_PKA_2 | 119 | 125 | PF00069 | 0.547 |
MOD_PKA_2 | 129 | 135 | PF00069 | 0.348 |
MOD_PKA_2 | 226 | 232 | PF00069 | 0.256 |
MOD_PKA_2 | 274 | 280 | PF00069 | 0.352 |
MOD_PKA_2 | 334 | 340 | PF00069 | 0.465 |
MOD_PKA_2 | 95 | 101 | PF00069 | 0.502 |
MOD_Plk_1 | 1 | 7 | PF00069 | 0.668 |
MOD_Plk_1 | 218 | 224 | PF00069 | 0.362 |
MOD_Plk_1 | 361 | 367 | PF00069 | 0.362 |
MOD_Plk_1 | 455 | 461 | PF00069 | 0.479 |
MOD_Plk_1 | 64 | 70 | PF00069 | 0.360 |
MOD_Plk_4 | 166 | 172 | PF00069 | 0.395 |
MOD_Plk_4 | 201 | 207 | PF00069 | 0.392 |
MOD_Plk_4 | 25 | 31 | PF00069 | 0.392 |
MOD_ProDKin_1 | 208 | 214 | PF00069 | 0.429 |
MOD_ProDKin_1 | 235 | 241 | PF00069 | 0.554 |
MOD_ProDKin_1 | 386 | 392 | PF00069 | 0.481 |
MOD_ProDKin_1 | 87 | 93 | PF00069 | 0.656 |
TRG_ENDOCYTIC_2 | 155 | 158 | PF00928 | 0.351 |
TRG_ENDOCYTIC_2 | 326 | 329 | PF00928 | 0.354 |
TRG_ENDOCYTIC_2 | 459 | 462 | PF00928 | 0.389 |
TRG_ER_diArg_1 | 274 | 276 | PF00400 | 0.457 |
TRG_ER_diArg_1 | 73 | 75 | PF00400 | 0.361 |
TRG_NES_CRM1_1 | 375 | 386 | PF08389 | 0.354 |
TRG_Pf-PMV_PEXEL_1 | 75 | 79 | PF00026 | 0.369 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I0M2 | Leptomonas seymouri | 65% | 100% |
A0A0N1PFX0 | Leptomonas seymouri | 36% | 100% |
A0A0S4J8Q0 | Bodo saltans | 39% | 100% |
A0A1X0NTE2 | Trypanosomatidae | 39% | 100% |
A0A1X0NX03 | Trypanosomatidae | 23% | 100% |
A0A3Q8IFK3 | Leishmania donovani | 90% | 100% |
A0A3S7WXD8 | Leishmania donovani | 47% | 100% |
A0A422NHR8 | Trypanosoma rangeli | 39% | 100% |
A4HCF4 | Leishmania braziliensis | 86% | 100% |
A4HZY3 | Leishmania infantum | 90% | 100% |
A4HZY4 | Leishmania infantum | 47% | 100% |
C9ZSM3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 100% |
C9ZVB8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 23% | 100% |
E9AVU5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 44% | 100% |
Q4QBN4 | Leishmania major | 45% | 100% |
Q4QBN5 | Leishmania major | 90% | 99% |
V5BJ96 | Trypanosoma cruzi | 24% | 100% |
V5BVW3 | Trypanosoma cruzi | 41% | 100% |