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: 8 |
NetGPI | no | yes: 0, no: 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9AXK5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 342 | 346 | PF00656 | 0.535 |
CLV_NRD_NRD_1 | 135 | 137 | PF00675 | 0.694 |
CLV_NRD_NRD_1 | 184 | 186 | PF00675 | 0.715 |
CLV_NRD_NRD_1 | 253 | 255 | PF00675 | 0.613 |
CLV_NRD_NRD_1 | 388 | 390 | PF00675 | 0.452 |
CLV_NRD_NRD_1 | 62 | 64 | PF00675 | 0.522 |
CLV_NRD_NRD_1 | 99 | 101 | PF00675 | 0.534 |
CLV_PCSK_KEX2_1 | 135 | 137 | PF00082 | 0.694 |
CLV_PCSK_KEX2_1 | 161 | 163 | PF00082 | 0.365 |
CLV_PCSK_KEX2_1 | 184 | 186 | PF00082 | 0.635 |
CLV_PCSK_KEX2_1 | 253 | 255 | PF00082 | 0.614 |
CLV_PCSK_KEX2_1 | 308 | 310 | PF00082 | 0.576 |
CLV_PCSK_KEX2_1 | 387 | 389 | PF00082 | 0.457 |
CLV_PCSK_KEX2_1 | 62 | 64 | PF00082 | 0.522 |
CLV_PCSK_KEX2_1 | 99 | 101 | PF00082 | 0.534 |
CLV_PCSK_PC1ET2_1 | 161 | 163 | PF00082 | 0.365 |
CLV_PCSK_PC1ET2_1 | 308 | 310 | PF00082 | 0.576 |
CLV_PCSK_PC7_1 | 384 | 390 | PF00082 | 0.545 |
CLV_PCSK_SKI1_1 | 238 | 242 | PF00082 | 0.402 |
CLV_PCSK_SKI1_1 | 309 | 313 | PF00082 | 0.569 |
CLV_PCSK_SKI1_1 | 80 | 84 | PF00082 | 0.450 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.476 |
DEG_SCF_FBW7_1 | 278 | 284 | PF00400 | 0.693 |
DEG_SCF_FBW7_1 | 408 | 414 | PF00400 | 0.605 |
DEG_SPOP_SBC_1 | 412 | 416 | PF00917 | 0.536 |
DEG_SPOP_SBC_1 | 481 | 485 | PF00917 | 0.798 |
DOC_CKS1_1 | 120 | 125 | PF01111 | 0.534 |
DOC_CKS1_1 | 278 | 283 | PF01111 | 0.691 |
DOC_CKS1_1 | 408 | 413 | PF01111 | 0.601 |
DOC_CKS1_1 | 442 | 447 | PF01111 | 0.654 |
DOC_USP7_MATH_1 | 15 | 19 | PF00917 | 0.519 |
DOC_USP7_MATH_1 | 173 | 177 | PF00917 | 0.549 |
DOC_USP7_MATH_1 | 214 | 218 | PF00917 | 0.645 |
DOC_USP7_MATH_1 | 262 | 266 | PF00917 | 0.626 |
DOC_USP7_MATH_1 | 279 | 283 | PF00917 | 0.645 |
DOC_USP7_MATH_1 | 324 | 328 | PF00917 | 0.562 |
DOC_USP7_MATH_1 | 411 | 415 | PF00917 | 0.683 |
DOC_USP7_MATH_1 | 450 | 454 | PF00917 | 0.679 |
DOC_USP7_MATH_1 | 481 | 485 | PF00917 | 0.729 |
DOC_USP7_MATH_1 | 91 | 95 | PF00917 | 0.408 |
DOC_WW_Pin1_4 | 115 | 120 | PF00397 | 0.698 |
DOC_WW_Pin1_4 | 129 | 134 | PF00397 | 0.694 |
DOC_WW_Pin1_4 | 200 | 205 | PF00397 | 0.715 |
DOC_WW_Pin1_4 | 215 | 220 | PF00397 | 0.654 |
DOC_WW_Pin1_4 | 221 | 226 | PF00397 | 0.646 |
DOC_WW_Pin1_4 | 248 | 253 | PF00397 | 0.438 |
DOC_WW_Pin1_4 | 268 | 273 | PF00397 | 0.824 |
DOC_WW_Pin1_4 | 277 | 282 | PF00397 | 0.669 |
DOC_WW_Pin1_4 | 407 | 412 | PF00397 | 0.730 |
DOC_WW_Pin1_4 | 413 | 418 | PF00397 | 0.605 |
DOC_WW_Pin1_4 | 441 | 446 | PF00397 | 0.667 |
DOC_WW_Pin1_4 | 459 | 464 | PF00397 | 0.727 |
DOC_WW_Pin1_4 | 87 | 92 | PF00397 | 0.476 |
LIG_14-3-3_CanoR_1 | 135 | 139 | PF00244 | 0.684 |
LIG_14-3-3_CanoR_1 | 162 | 167 | PF00244 | 0.515 |
LIG_14-3-3_CanoR_1 | 174 | 178 | PF00244 | 0.573 |
LIG_14-3-3_CanoR_1 | 213 | 219 | PF00244 | 0.828 |
LIG_14-3-3_CanoR_1 | 227 | 236 | PF00244 | 0.323 |
LIG_14-3-3_CanoR_1 | 242 | 248 | PF00244 | 0.349 |
LIG_14-3-3_CanoR_1 | 290 | 300 | PF00244 | 0.790 |
LIG_14-3-3_CanoR_1 | 309 | 318 | PF00244 | 0.378 |
LIG_14-3-3_CanoR_1 | 457 | 466 | PF00244 | 0.538 |
LIG_BRCT_BRCA1_1 | 19 | 23 | PF00533 | 0.523 |
LIG_BRCT_BRCA1_1 | 5 | 9 | PF00533 | 0.514 |
LIG_CaM_IQ_9 | 376 | 391 | PF13499 | 0.547 |
LIG_FHA_1 | 191 | 197 | PF00498 | 0.497 |
LIG_FHA_1 | 342 | 348 | PF00498 | 0.579 |
LIG_FHA_1 | 68 | 74 | PF00498 | 0.505 |
LIG_FHA_2 | 293 | 299 | PF00498 | 0.630 |
LIG_FHA_2 | 486 | 492 | PF00498 | 0.709 |
LIG_FHA_2 | 495 | 501 | PF00498 | 0.699 |
LIG_Integrin_RGD_1 | 37 | 39 | PF01839 | 0.603 |
LIG_LIR_Apic_2 | 68 | 74 | PF02991 | 0.446 |
LIG_LIR_Gen_1 | 154 | 163 | PF02991 | 0.462 |
LIG_LIR_Gen_1 | 175 | 183 | PF02991 | 0.504 |
LIG_LIR_Gen_1 | 297 | 307 | PF02991 | 0.628 |
LIG_LIR_Gen_1 | 499 | 509 | PF02991 | 0.583 |
LIG_LIR_Gen_1 | 6 | 16 | PF02991 | 0.491 |
LIG_LIR_Nem_3 | 154 | 158 | PF02991 | 0.472 |
LIG_LIR_Nem_3 | 175 | 181 | PF02991 | 0.498 |
LIG_LIR_Nem_3 | 20 | 26 | PF02991 | 0.562 |
LIG_LIR_Nem_3 | 233 | 239 | PF02991 | 0.353 |
LIG_LIR_Nem_3 | 297 | 303 | PF02991 | 0.649 |
LIG_LIR_Nem_3 | 6 | 12 | PF02991 | 0.484 |
LIG_Pex14_2 | 12 | 16 | PF04695 | 0.511 |
LIG_Pex14_2 | 236 | 240 | PF04695 | 0.309 |
LIG_REV1ctd_RIR_1 | 233 | 242 | PF16727 | 0.358 |
LIG_SH2_CRK | 163 | 167 | PF00017 | 0.419 |
LIG_SH2_CRK | 71 | 75 | PF00017 | 0.480 |
LIG_SH2_SRC | 26 | 29 | PF00017 | 0.513 |
LIG_SH2_STAT5 | 239 | 242 | PF00017 | 0.343 |
LIG_SH2_STAT5 | 26 | 29 | PF00017 | 0.571 |
LIG_SH2_STAT5 | 71 | 74 | PF00017 | 0.395 |
LIG_SH3_1 | 71 | 77 | PF00018 | 0.446 |
LIG_SH3_3 | 117 | 123 | PF00018 | 0.493 |
LIG_SH3_3 | 135 | 141 | PF00018 | 0.711 |
LIG_SH3_3 | 213 | 219 | PF00018 | 0.647 |
LIG_SH3_3 | 269 | 275 | PF00018 | 0.742 |
LIG_SH3_3 | 414 | 420 | PF00018 | 0.646 |
LIG_SH3_3 | 439 | 445 | PF00018 | 0.719 |
LIG_SH3_3 | 460 | 466 | PF00018 | 0.706 |
LIG_SH3_3 | 71 | 77 | PF00018 | 0.484 |
LIG_TRAF2_1 | 144 | 147 | PF00917 | 0.488 |
LIG_TRAF2_1 | 496 | 499 | PF00917 | 0.547 |
LIG_TYR_ITIM | 153 | 158 | PF00017 | 0.476 |
MOD_CDC14_SPxK_1 | 251 | 254 | PF00782 | 0.403 |
MOD_CDK_SPK_2 | 248 | 253 | PF00069 | 0.365 |
MOD_CDK_SPxK_1 | 119 | 125 | PF00069 | 0.568 |
MOD_CDK_SPxK_1 | 129 | 135 | PF00069 | 0.677 |
MOD_CDK_SPxK_1 | 221 | 227 | PF00069 | 0.712 |
MOD_CDK_SPxK_1 | 248 | 254 | PF00069 | 0.373 |
MOD_CDK_SPxxK_3 | 129 | 136 | PF00069 | 0.678 |
MOD_CK1_1 | 217 | 223 | PF00069 | 0.791 |
MOD_CK1_1 | 263 | 269 | PF00069 | 0.705 |
MOD_CK1_1 | 271 | 277 | PF00069 | 0.724 |
MOD_CK1_1 | 291 | 297 | PF00069 | 0.500 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.554 |
MOD_CK1_1 | 334 | 340 | PF00069 | 0.662 |
MOD_CK1_1 | 427 | 433 | PF00069 | 0.655 |
MOD_CK1_1 | 479 | 485 | PF00069 | 0.803 |
MOD_CK1_1 | 494 | 500 | PF00069 | 0.540 |
MOD_CK1_1 | 90 | 96 | PF00069 | 0.413 |
MOD_CK2_1 | 109 | 115 | PF00069 | 0.686 |
MOD_CK2_1 | 228 | 234 | PF00069 | 0.464 |
MOD_CK2_1 | 292 | 298 | PF00069 | 0.597 |
MOD_CK2_1 | 334 | 340 | PF00069 | 0.611 |
MOD_CK2_1 | 392 | 398 | PF00069 | 0.381 |
MOD_CK2_1 | 504 | 510 | PF00069 | 0.618 |
MOD_GlcNHglycan | 19 | 22 | PF01048 | 0.491 |
MOD_GlcNHglycan | 220 | 223 | PF01048 | 0.773 |
MOD_GlcNHglycan | 262 | 265 | PF01048 | 0.636 |
MOD_GlcNHglycan | 266 | 269 | PF01048 | 0.584 |
MOD_GlcNHglycan | 314 | 317 | PF01048 | 0.495 |
MOD_GlcNHglycan | 336 | 339 | PF01048 | 0.611 |
MOD_GlcNHglycan | 394 | 397 | PF01048 | 0.512 |
MOD_GlcNHglycan | 453 | 456 | PF01048 | 0.756 |
MOD_GlcNHglycan | 459 | 462 | PF01048 | 0.656 |
MOD_GlcNHglycan | 488 | 491 | PF01048 | 0.724 |
MOD_GlcNHglycan | 493 | 496 | PF01048 | 0.660 |
MOD_GlcNHglycan | 93 | 96 | PF01048 | 0.442 |
MOD_GSK3_1 | 107 | 114 | PF00069 | 0.676 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.782 |
MOD_GSK3_1 | 173 | 180 | PF00069 | 0.566 |
MOD_GSK3_1 | 214 | 221 | PF00069 | 0.675 |
MOD_GSK3_1 | 260 | 267 | PF00069 | 0.693 |
MOD_GSK3_1 | 273 | 280 | PF00069 | 0.733 |
MOD_GSK3_1 | 288 | 295 | PF00069 | 0.772 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.498 |
MOD_GSK3_1 | 341 | 348 | PF00069 | 0.750 |
MOD_GSK3_1 | 407 | 414 | PF00069 | 0.729 |
MOD_GSK3_1 | 476 | 483 | PF00069 | 0.740 |
MOD_GSK3_1 | 494 | 501 | PF00069 | 0.594 |
MOD_GSK3_1 | 87 | 94 | PF00069 | 0.426 |
MOD_NEK2_1 | 241 | 246 | PF00069 | 0.384 |
MOD_PIKK_1 | 241 | 247 | PF00454 | 0.444 |
MOD_PIKK_1 | 3 | 9 | PF00454 | 0.522 |
MOD_PKA_2 | 134 | 140 | PF00069 | 0.680 |
MOD_PKA_2 | 173 | 179 | PF00069 | 0.591 |
MOD_PKA_2 | 228 | 234 | PF00069 | 0.443 |
MOD_PKA_2 | 241 | 247 | PF00069 | 0.338 |
MOD_PKA_2 | 291 | 297 | PF00069 | 0.763 |
MOD_PKA_2 | 334 | 340 | PF00069 | 0.584 |
MOD_PKA_2 | 435 | 441 | PF00069 | 0.638 |
MOD_PKB_1 | 290 | 298 | PF00069 | 0.724 |
MOD_Plk_1 | 424 | 430 | PF00069 | 0.681 |
MOD_Plk_1 | 498 | 504 | PF00069 | 0.625 |
MOD_Plk_1 | 67 | 73 | PF00069 | 0.569 |
MOD_Plk_2-3 | 345 | 351 | PF00069 | 0.617 |
MOD_Plk_4 | 162 | 168 | PF00069 | 0.495 |
MOD_Plk_4 | 173 | 179 | PF00069 | 0.672 |
MOD_Plk_4 | 324 | 330 | PF00069 | 0.546 |
MOD_Plk_4 | 371 | 377 | PF00069 | 0.422 |
MOD_Plk_4 | 498 | 504 | PF00069 | 0.730 |
MOD_ProDKin_1 | 115 | 121 | PF00069 | 0.697 |
MOD_ProDKin_1 | 129 | 135 | PF00069 | 0.694 |
MOD_ProDKin_1 | 200 | 206 | PF00069 | 0.713 |
MOD_ProDKin_1 | 215 | 221 | PF00069 | 0.655 |
MOD_ProDKin_1 | 248 | 254 | PF00069 | 0.446 |
MOD_ProDKin_1 | 268 | 274 | PF00069 | 0.825 |
MOD_ProDKin_1 | 277 | 283 | PF00069 | 0.671 |
MOD_ProDKin_1 | 407 | 413 | PF00069 | 0.734 |
MOD_ProDKin_1 | 441 | 447 | PF00069 | 0.669 |
MOD_ProDKin_1 | 459 | 465 | PF00069 | 0.728 |
MOD_ProDKin_1 | 87 | 93 | PF00069 | 0.469 |
MOD_SUMO_for_1 | 16 | 19 | PF00179 | 0.521 |
MOD_SUMO_rev_2 | 349 | 359 | PF00179 | 0.692 |
MOD_SUMO_rev_2 | 395 | 402 | PF00179 | 0.345 |
TRG_AP2beta_CARGO_1 | 237 | 247 | PF09066 | 0.330 |
TRG_DiLeu_BaEn_2 | 18 | 24 | PF01217 | 0.524 |
TRG_DiLeu_BaLyEn_6 | 148 | 153 | PF01217 | 0.393 |
TRG_ENDOCYTIC_2 | 155 | 158 | PF00928 | 0.506 |
TRG_ENDOCYTIC_2 | 163 | 166 | PF00928 | 0.392 |
TRG_ER_diArg_1 | 149 | 152 | PF00400 | 0.370 |
TRG_ER_diArg_1 | 184 | 186 | PF00400 | 0.639 |
TRG_ER_diArg_1 | 227 | 230 | PF00400 | 0.515 |
TRG_ER_diArg_1 | 252 | 254 | PF00400 | 0.606 |
TRG_ER_diArg_1 | 387 | 389 | PF00400 | 0.497 |
TRG_ER_diArg_1 | 61 | 63 | PF00400 | 0.522 |
TRG_ER_diArg_1 | 98 | 100 | PF00400 | 0.481 |
TRG_Pf-PMV_PEXEL_1 | 62 | 66 | PF00026 | 0.535 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PC05 | Leptomonas seymouri | 47% | 94% |
A0A1X0NLY0 | Trypanosomatidae | 27% | 100% |
A0A3R7NU60 | Trypanosoma rangeli | 28% | 100% |
A0A3S7WZ41 | Leishmania donovani | 89% | 100% |
A4HE69 | Leishmania braziliensis | 66% | 98% |
A4I1H1 | Leishmania infantum | 89% | 100% |
Q4Q9W6 | Leishmania major | 90% | 100% |