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: 7 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 2 |
GO:0016020 | membrane | 2 | 7 |
GO:0031974 | membrane-enclosed lumen | 2 | 2 |
GO:0031981 | nuclear lumen | 5 | 2 |
GO:0032838 | plasma membrane bounded cell projection cytoplasm | 4 | 2 |
GO:0043233 | organelle lumen | 3 | 2 |
GO:0070013 | intracellular organelle lumen | 4 | 2 |
GO:0097014 | ciliary plasm | 5 | 2 |
GO:0099568 | cytoplasmic region | 3 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 7 |
Related structures:
AlphaFold database: E9ADT6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 39 | 43 | PF00656 | 0.562 |
CLV_NRD_NRD_1 | 245 | 247 | PF00675 | 0.641 |
CLV_NRD_NRD_1 | 361 | 363 | PF00675 | 0.735 |
CLV_NRD_NRD_1 | 474 | 476 | PF00675 | 0.510 |
CLV_PCSK_KEX2_1 | 245 | 247 | PF00082 | 0.641 |
CLV_PCSK_KEX2_1 | 361 | 363 | PF00082 | 0.762 |
CLV_PCSK_KEX2_1 | 474 | 476 | PF00082 | 0.453 |
CLV_PCSK_SKI1_1 | 208 | 212 | PF00082 | 0.584 |
CLV_PCSK_SKI1_1 | 228 | 232 | PF00082 | 0.549 |
CLV_PCSK_SKI1_1 | 237 | 241 | PF00082 | 0.581 |
CLV_PCSK_SKI1_1 | 26 | 30 | PF00082 | 0.749 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.566 |
DOC_CDC14_PxL_1 | 272 | 280 | PF14671 | 0.408 |
DOC_CDC14_PxL_1 | 342 | 350 | PF14671 | 0.540 |
DOC_MAPK_gen_1 | 215 | 223 | PF00069 | 0.377 |
DOC_MAPK_HePTP_8 | 450 | 462 | PF00069 | 0.318 |
DOC_MAPK_MEF2A_6 | 453 | 462 | PF00069 | 0.377 |
DOC_USP7_MATH_1 | 138 | 142 | PF00917 | 0.548 |
DOC_USP7_MATH_1 | 235 | 239 | PF00917 | 0.421 |
DOC_USP7_MATH_1 | 259 | 263 | PF00917 | 0.439 |
DOC_USP7_MATH_1 | 356 | 360 | PF00917 | 0.538 |
DOC_USP7_MATH_1 | 6 | 10 | PF00917 | 0.570 |
DOC_USP7_UBL2_3 | 179 | 183 | PF12436 | 0.483 |
DOC_WW_Pin1_4 | 346 | 351 | PF00397 | 0.564 |
DOC_WW_Pin1_4 | 37 | 42 | PF00397 | 0.566 |
DOC_WW_Pin1_4 | 426 | 431 | PF00397 | 0.596 |
DOC_WW_Pin1_4 | 445 | 450 | PF00397 | 0.529 |
LIG_14-3-3_CanoR_1 | 169 | 174 | PF00244 | 0.381 |
LIG_14-3-3_CanoR_1 | 453 | 458 | PF00244 | 0.377 |
LIG_14-3-3_CanoR_1 | 474 | 481 | PF00244 | 0.591 |
LIG_14-3-3_CanoR_1 | 5 | 11 | PF00244 | 0.434 |
LIG_Actin_WH2_2 | 264 | 281 | PF00022 | 0.351 |
LIG_BRCT_BRCA1_1 | 455 | 459 | PF00533 | 0.282 |
LIG_deltaCOP1_diTrp_1 | 298 | 308 | PF00928 | 0.437 |
LIG_FHA_1 | 107 | 113 | PF00498 | 0.444 |
LIG_FHA_2 | 258 | 264 | PF00498 | 0.461 |
LIG_FHA_2 | 82 | 88 | PF00498 | 0.552 |
LIG_Integrin_RGD_1 | 327 | 329 | PF01839 | 0.686 |
LIG_LIR_Apic_2 | 399 | 405 | PF02991 | 0.486 |
LIG_LIR_Gen_1 | 214 | 223 | PF02991 | 0.336 |
LIG_LIR_Gen_1 | 456 | 467 | PF02991 | 0.282 |
LIG_LIR_Nem_3 | 214 | 219 | PF02991 | 0.342 |
LIG_LIR_Nem_3 | 269 | 275 | PF02991 | 0.467 |
LIG_LIR_Nem_3 | 319 | 325 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 451 | 455 | PF02991 | 0.391 |
LIG_LIR_Nem_3 | 456 | 462 | PF02991 | 0.396 |
LIG_MYND_1 | 346 | 350 | PF01753 | 0.544 |
LIG_NRBOX | 457 | 463 | PF00104 | 0.397 |
LIG_PDZ_Class_1 | 479 | 484 | PF00595 | 0.590 |
LIG_SH2_CRK | 452 | 456 | PF00017 | 0.318 |
LIG_SH2_PTP2 | 402 | 405 | PF00017 | 0.529 |
LIG_SH2_SRC | 173 | 176 | PF00017 | 0.449 |
LIG_SH2_STAT5 | 16 | 19 | PF00017 | 0.446 |
LIG_SH2_STAT5 | 173 | 176 | PF00017 | 0.394 |
LIG_SH2_STAT5 | 282 | 285 | PF00017 | 0.393 |
LIG_SH2_STAT5 | 331 | 334 | PF00017 | 0.537 |
LIG_SH2_STAT5 | 402 | 405 | PF00017 | 0.529 |
LIG_SH3_2 | 335 | 340 | PF14604 | 0.531 |
LIG_SH3_3 | 220 | 226 | PF00018 | 0.380 |
LIG_SH3_3 | 270 | 276 | PF00018 | 0.396 |
LIG_SH3_3 | 332 | 338 | PF00018 | 0.501 |
LIG_SH3_3 | 347 | 353 | PF00018 | 0.508 |
LIG_SH3_3 | 38 | 44 | PF00018 | 0.508 |
LIG_SH3_3 | 424 | 430 | PF00018 | 0.521 |
LIG_SUMO_SIM_par_1 | 147 | 154 | PF11976 | 0.462 |
LIG_SUMO_SIM_par_1 | 9 | 15 | PF11976 | 0.536 |
LIG_TRAF2_1 | 119 | 122 | PF00917 | 0.515 |
LIG_TRAF2_1 | 124 | 127 | PF00917 | 0.570 |
LIG_TRAF2_2 | 353 | 358 | PF00917 | 0.591 |
LIG_TYR_ITIM | 450 | 455 | PF00017 | 0.476 |
MOD_CDK_SPxK_1 | 346 | 352 | PF00069 | 0.544 |
MOD_CK1_1 | 141 | 147 | PF00069 | 0.540 |
MOD_CK1_1 | 40 | 46 | PF00069 | 0.558 |
MOD_CK1_1 | 406 | 412 | PF00069 | 0.600 |
MOD_CK1_1 | 415 | 421 | PF00069 | 0.559 |
MOD_CK1_1 | 9 | 15 | PF00069 | 0.582 |
MOD_GlcNHglycan | 139 | 143 | PF01048 | 0.743 |
MOD_GlcNHglycan | 162 | 165 | PF01048 | 0.631 |
MOD_GlcNHglycan | 408 | 411 | PF01048 | 0.734 |
MOD_GlcNHglycan | 420 | 423 | PF01048 | 0.701 |
MOD_GlcNHglycan | 469 | 472 | PF01048 | 0.257 |
MOD_GSK3_1 | 138 | 145 | PF00069 | 0.576 |
MOD_GSK3_1 | 300 | 307 | PF00069 | 0.434 |
MOD_GSK3_1 | 311 | 318 | PF00069 | 0.457 |
MOD_GSK3_1 | 33 | 40 | PF00069 | 0.600 |
MOD_GSK3_1 | 56 | 63 | PF00069 | 0.551 |
MOD_N-GLC_1 | 329 | 334 | PF02516 | 0.774 |
MOD_NEK2_1 | 151 | 156 | PF00069 | 0.436 |
MOD_NEK2_1 | 203 | 208 | PF00069 | 0.373 |
MOD_NEK2_1 | 467 | 472 | PF00069 | 0.377 |
MOD_NEK2_1 | 60 | 65 | PF00069 | 0.521 |
MOD_NEK2_2 | 235 | 240 | PF00069 | 0.409 |
MOD_PIKK_1 | 300 | 306 | PF00454 | 0.428 |
MOD_PIKK_1 | 403 | 409 | PF00454 | 0.559 |
MOD_PK_1 | 453 | 459 | PF00069 | 0.377 |
MOD_PKA_1 | 474 | 480 | PF00069 | 0.622 |
MOD_PKA_2 | 309 | 315 | PF00069 | 0.423 |
MOD_PKA_2 | 375 | 381 | PF00069 | 0.503 |
MOD_PKA_2 | 383 | 389 | PF00069 | 0.502 |
MOD_PKA_2 | 418 | 424 | PF00069 | 0.541 |
MOD_PKA_2 | 474 | 480 | PF00069 | 0.658 |
MOD_Plk_1 | 56 | 62 | PF00069 | 0.593 |
MOD_Plk_2-3 | 106 | 112 | PF00069 | 0.506 |
MOD_Plk_2-3 | 56 | 62 | PF00069 | 0.560 |
MOD_Plk_4 | 169 | 175 | PF00069 | 0.432 |
MOD_Plk_4 | 193 | 199 | PF00069 | 0.416 |
MOD_Plk_4 | 453 | 459 | PF00069 | 0.397 |
MOD_Plk_4 | 6 | 12 | PF00069 | 0.461 |
MOD_ProDKin_1 | 346 | 352 | PF00069 | 0.563 |
MOD_ProDKin_1 | 37 | 43 | PF00069 | 0.566 |
MOD_ProDKin_1 | 426 | 432 | PF00069 | 0.596 |
MOD_ProDKin_1 | 445 | 451 | PF00069 | 0.522 |
MOD_SUMO_for_1 | 296 | 299 | PF00179 | 0.418 |
TRG_ENDOCYTIC_2 | 452 | 455 | PF00928 | 0.413 |
TRG_ER_diArg_1 | 361 | 364 | PF00400 | 0.535 |
TRG_ER_diArg_1 | 379 | 382 | PF00400 | 0.459 |
TRG_ER_diArg_1 | 473 | 475 | PF00400 | 0.630 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8Q7 | Leptomonas seymouri | 58% | 96% |
A0A3S7X2C7 | Leishmania donovani | 91% | 100% |
A4HH91 | Leishmania braziliensis | 70% | 100% |
A4I4D7 | Leishmania infantum | 92% | 100% |
C9ZL27 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 99% |
E9ALZ4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |