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 |
Related structures:
AlphaFold database: Q4QBT7
Term | Name | Level | Count |
---|---|---|---|
GO:0006473 | protein acetylation | 6 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0019538 | protein metabolic process | 3 | 2 |
GO:0036211 | protein modification process | 4 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0043412 | macromolecule modification | 4 | 2 |
GO:0043543 | protein acylation | 5 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 8 |
GO:0008080 | N-acetyltransferase activity | 6 | 8 |
GO:0016407 | acetyltransferase activity | 5 | 8 |
GO:0016410 | N-acyltransferase activity | 5 | 8 |
GO:0016740 | transferase activity | 2 | 8 |
GO:0016746 | acyltransferase activity | 3 | 8 |
GO:0016747 | acyltransferase activity, transferring groups other than amino-acyl groups | 4 | 8 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 270 | 274 | PF00656 | 0.509 |
CLV_NRD_NRD_1 | 247 | 249 | PF00675 | 0.516 |
CLV_NRD_NRD_1 | 335 | 337 | PF00675 | 0.319 |
CLV_NRD_NRD_1 | 404 | 406 | PF00675 | 0.628 |
CLV_NRD_NRD_1 | 412 | 414 | PF00675 | 0.636 |
CLV_PCSK_KEX2_1 | 213 | 215 | PF00082 | 0.605 |
CLV_PCSK_KEX2_1 | 247 | 249 | PF00082 | 0.516 |
CLV_PCSK_KEX2_1 | 334 | 336 | PF00082 | 0.317 |
CLV_PCSK_KEX2_1 | 404 | 406 | PF00082 | 0.590 |
CLV_PCSK_KEX2_1 | 412 | 414 | PF00082 | 0.612 |
CLV_PCSK_PC1ET2_1 | 213 | 215 | PF00082 | 0.627 |
CLV_PCSK_SKI1_1 | 221 | 225 | PF00082 | 0.616 |
CLV_PCSK_SKI1_1 | 247 | 251 | PF00082 | 0.618 |
CLV_PCSK_SKI1_1 | 384 | 388 | PF00082 | 0.467 |
CLV_PCSK_SKI1_1 | 486 | 490 | PF00082 | 0.787 |
DEG_APCC_DBOX_1 | 5 | 13 | PF00400 | 0.592 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.583 |
DEG_ODPH_VHL_1 | 316 | 328 | PF01847 | 0.555 |
DOC_CDC14_PxL_1 | 48 | 56 | PF14671 | 0.453 |
DOC_CKS1_1 | 309 | 314 | PF01111 | 0.608 |
DOC_CYCLIN_RxL_1 | 137 | 147 | PF00134 | 0.546 |
DOC_CYCLIN_RxL_1 | 218 | 228 | PF00134 | 0.646 |
DOC_CYCLIN_yCln2_LP_2 | 102 | 108 | PF00134 | 0.521 |
DOC_MAPK_gen_1 | 384 | 394 | PF00069 | 0.561 |
DOC_MAPK_MEF2A_6 | 320 | 328 | PF00069 | 0.556 |
DOC_PP1_RVXF_1 | 375 | 381 | PF00149 | 0.452 |
DOC_PP2B_LxvP_1 | 102 | 105 | PF13499 | 0.485 |
DOC_PP4_FxxP_1 | 169 | 172 | PF00568 | 0.700 |
DOC_USP7_MATH_1 | 111 | 115 | PF00917 | 0.512 |
DOC_USP7_MATH_1 | 156 | 160 | PF00917 | 0.711 |
DOC_USP7_MATH_1 | 162 | 166 | PF00917 | 0.715 |
DOC_USP7_MATH_1 | 174 | 178 | PF00917 | 0.627 |
DOC_USP7_MATH_1 | 301 | 305 | PF00917 | 0.601 |
DOC_USP7_MATH_1 | 420 | 424 | PF00917 | 0.642 |
DOC_USP7_MATH_1 | 441 | 445 | PF00917 | 0.704 |
DOC_USP7_MATH_1 | 73 | 77 | PF00917 | 0.574 |
DOC_USP7_MATH_2 | 450 | 456 | PF00917 | 0.607 |
DOC_WW_Pin1_4 | 117 | 122 | PF00397 | 0.578 |
DOC_WW_Pin1_4 | 158 | 163 | PF00397 | 0.733 |
DOC_WW_Pin1_4 | 293 | 298 | PF00397 | 0.555 |
DOC_WW_Pin1_4 | 304 | 309 | PF00397 | 0.567 |
DOC_WW_Pin1_4 | 31 | 36 | PF00397 | 0.452 |
DOC_WW_Pin1_4 | 4 | 9 | PF00397 | 0.600 |
DOC_WW_Pin1_4 | 432 | 437 | PF00397 | 0.578 |
DOC_WW_Pin1_4 | 472 | 477 | PF00397 | 0.513 |
LIG_14-3-3_CanoR_1 | 11 | 17 | PF00244 | 0.575 |
LIG_14-3-3_CanoR_1 | 140 | 145 | PF00244 | 0.610 |
LIG_14-3-3_CanoR_1 | 201 | 210 | PF00244 | 0.671 |
LIG_14-3-3_CanoR_1 | 295 | 303 | PF00244 | 0.581 |
LIG_14-3-3_CanoR_1 | 418 | 426 | PF00244 | 0.571 |
LIG_APCC_ABBA_1 | 371 | 376 | PF00400 | 0.536 |
LIG_APCC_ABBA_1 | 380 | 385 | PF00400 | 0.469 |
LIG_APCC_ABBA_1 | 386 | 391 | PF00400 | 0.437 |
LIG_BRCT_BRCA1_1 | 318 | 322 | PF00533 | 0.556 |
LIG_Clathr_ClatBox_1 | 262 | 266 | PF01394 | 0.555 |
LIG_EH1_1 | 321 | 329 | PF00400 | 0.556 |
LIG_FHA_1 | 187 | 193 | PF00498 | 0.678 |
LIG_FHA_1 | 319 | 325 | PF00498 | 0.556 |
LIG_FHA_1 | 355 | 361 | PF00498 | 0.536 |
LIG_FHA_1 | 366 | 372 | PF00498 | 0.482 |
LIG_FHA_1 | 373 | 379 | PF00498 | 0.470 |
LIG_FHA_1 | 5 | 11 | PF00498 | 0.484 |
LIG_FHA_1 | 97 | 103 | PF00498 | 0.421 |
LIG_FHA_2 | 182 | 188 | PF00498 | 0.663 |
LIG_FHA_2 | 189 | 195 | PF00498 | 0.764 |
LIG_FHA_2 | 398 | 404 | PF00498 | 0.540 |
LIG_FHA_2 | 72 | 78 | PF00498 | 0.522 |
LIG_LIR_Apic_2 | 168 | 172 | PF02991 | 0.709 |
LIG_LIR_Apic_2 | 471 | 476 | PF02991 | 0.698 |
LIG_LIR_Gen_1 | 253 | 262 | PF02991 | 0.306 |
LIG_LIR_Gen_1 | 99 | 108 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 253 | 257 | PF02991 | 0.328 |
LIG_LIR_Nem_3 | 99 | 103 | PF02991 | 0.413 |
LIG_MYND_1 | 308 | 312 | PF01753 | 0.529 |
LIG_MYND_1 | 52 | 56 | PF01753 | 0.540 |
LIG_MYND_3 | 148 | 152 | PF01753 | 0.694 |
LIG_SH2_PTP2 | 254 | 257 | PF00017 | 0.411 |
LIG_SH2_SRC | 215 | 218 | PF00017 | 0.700 |
LIG_SH2_STAP1 | 188 | 192 | PF00017 | 0.587 |
LIG_SH2_STAP1 | 349 | 353 | PF00017 | 0.556 |
LIG_SH2_STAT5 | 188 | 191 | PF00017 | 0.576 |
LIG_SH2_STAT5 | 254 | 257 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 53 | 56 | PF00017 | 0.467 |
LIG_SH3_1 | 53 | 59 | PF00018 | 0.542 |
LIG_SH3_3 | 173 | 179 | PF00018 | 0.712 |
LIG_SH3_3 | 29 | 35 | PF00018 | 0.538 |
LIG_SH3_3 | 306 | 312 | PF00018 | 0.608 |
LIG_SH3_3 | 325 | 331 | PF00018 | 0.411 |
LIG_SH3_3 | 46 | 52 | PF00018 | 0.400 |
LIG_SH3_3 | 53 | 59 | PF00018 | 0.459 |
LIG_SUMO_SIM_anti_2 | 323 | 328 | PF11976 | 0.556 |
LIG_SUMO_SIM_anti_2 | 47 | 52 | PF11976 | 0.508 |
LIG_SUMO_SIM_par_1 | 74 | 84 | PF11976 | 0.543 |
LIG_TRAF2_1 | 150 | 153 | PF00917 | 0.698 |
LIG_TRAF2_1 | 80 | 83 | PF00917 | 0.483 |
LIG_UBA3_1 | 89 | 97 | PF00899 | 0.380 |
LIG_WRC_WIRS_1 | 166 | 171 | PF05994 | 0.702 |
MOD_CDC14_SPxK_1 | 120 | 123 | PF00782 | 0.592 |
MOD_CDK_SPxK_1 | 117 | 123 | PF00069 | 0.593 |
MOD_CDK_SPxxK_3 | 4 | 11 | PF00069 | 0.596 |
MOD_CDK_SPxxK_3 | 472 | 479 | PF00069 | 0.497 |
MOD_CK1_1 | 165 | 171 | PF00069 | 0.723 |
MOD_CK1_1 | 181 | 187 | PF00069 | 0.662 |
MOD_CK1_1 | 225 | 231 | PF00069 | 0.690 |
MOD_CK1_1 | 296 | 302 | PF00069 | 0.596 |
MOD_CK1_1 | 304 | 310 | PF00069 | 0.549 |
MOD_CK1_1 | 397 | 403 | PF00069 | 0.611 |
MOD_CK1_1 | 422 | 428 | PF00069 | 0.732 |
MOD_CK1_1 | 444 | 450 | PF00069 | 0.597 |
MOD_CK1_1 | 466 | 472 | PF00069 | 0.622 |
MOD_CK2_1 | 188 | 194 | PF00069 | 0.749 |
MOD_CK2_1 | 283 | 289 | PF00069 | 0.562 |
MOD_CK2_1 | 397 | 403 | PF00069 | 0.538 |
MOD_CK2_1 | 71 | 77 | PF00069 | 0.510 |
MOD_DYRK1A_RPxSP_1 | 31 | 35 | PF00069 | 0.434 |
MOD_GlcNHglycan | 112 | 116 | PF01048 | 0.649 |
MOD_GlcNHglycan | 12 | 15 | PF01048 | 0.576 |
MOD_GlcNHglycan | 204 | 207 | PF01048 | 0.679 |
MOD_GlcNHglycan | 229 | 232 | PF01048 | 0.729 |
MOD_GlcNHglycan | 298 | 301 | PF01048 | 0.375 |
MOD_GlcNHglycan | 313 | 316 | PF01048 | 0.217 |
MOD_GlcNHglycan | 422 | 425 | PF01048 | 0.685 |
MOD_GlcNHglycan | 454 | 457 | PF01048 | 0.833 |
MOD_GSK3_1 | 140 | 147 | PF00069 | 0.617 |
MOD_GSK3_1 | 154 | 161 | PF00069 | 0.675 |
MOD_GSK3_1 | 174 | 181 | PF00069 | 0.640 |
MOD_GSK3_1 | 182 | 189 | PF00069 | 0.598 |
MOD_GSK3_1 | 223 | 230 | PF00069 | 0.669 |
MOD_GSK3_1 | 291 | 298 | PF00069 | 0.582 |
MOD_GSK3_1 | 304 | 311 | PF00069 | 0.535 |
MOD_GSK3_1 | 363 | 370 | PF00069 | 0.504 |
MOD_GSK3_1 | 416 | 423 | PF00069 | 0.547 |
MOD_GSK3_1 | 468 | 475 | PF00069 | 0.584 |
MOD_GSK3_1 | 73 | 80 | PF00069 | 0.517 |
MOD_GSK3_1 | 92 | 99 | PF00069 | 0.451 |
MOD_LATS_1 | 138 | 144 | PF00433 | 0.545 |
MOD_LATS_1 | 293 | 299 | PF00433 | 0.529 |
MOD_NEK2_1 | 10 | 15 | PF00069 | 0.579 |
MOD_NEK2_1 | 144 | 149 | PF00069 | 0.679 |
MOD_NEK2_1 | 21 | 26 | PF00069 | 0.481 |
MOD_NEK2_1 | 250 | 255 | PF00069 | 0.581 |
MOD_NEK2_1 | 282 | 287 | PF00069 | 0.529 |
MOD_NEK2_1 | 394 | 399 | PF00069 | 0.562 |
MOD_NEK2_1 | 468 | 473 | PF00069 | 0.635 |
MOD_PIKK_1 | 215 | 221 | PF00454 | 0.705 |
MOD_PIKK_1 | 230 | 236 | PF00454 | 0.589 |
MOD_PIKK_1 | 42 | 48 | PF00454 | 0.363 |
MOD_PIKK_1 | 458 | 464 | PF00454 | 0.730 |
MOD_PIKK_1 | 486 | 492 | PF00454 | 0.787 |
MOD_PKA_2 | 10 | 16 | PF00069 | 0.578 |
MOD_PKA_2 | 200 | 206 | PF00069 | 0.685 |
MOD_PKA_2 | 411 | 417 | PF00069 | 0.634 |
MOD_PKA_2 | 444 | 450 | PF00069 | 0.707 |
MOD_PKB_1 | 199 | 207 | PF00069 | 0.716 |
MOD_Plk_1 | 111 | 117 | PF00069 | 0.543 |
MOD_Plk_2-3 | 77 | 83 | PF00069 | 0.516 |
MOD_Plk_4 | 12 | 18 | PF00069 | 0.571 |
MOD_Plk_4 | 178 | 184 | PF00069 | 0.622 |
MOD_Plk_4 | 250 | 256 | PF00069 | 0.462 |
MOD_Plk_4 | 468 | 474 | PF00069 | 0.615 |
MOD_Plk_4 | 96 | 102 | PF00069 | 0.410 |
MOD_ProDKin_1 | 117 | 123 | PF00069 | 0.581 |
MOD_ProDKin_1 | 158 | 164 | PF00069 | 0.733 |
MOD_ProDKin_1 | 293 | 299 | PF00069 | 0.555 |
MOD_ProDKin_1 | 304 | 310 | PF00069 | 0.567 |
MOD_ProDKin_1 | 31 | 37 | PF00069 | 0.446 |
MOD_ProDKin_1 | 4 | 10 | PF00069 | 0.598 |
MOD_ProDKin_1 | 432 | 438 | PF00069 | 0.581 |
MOD_ProDKin_1 | 472 | 478 | PF00069 | 0.515 |
TRG_DiLeu_BaEn_1 | 39 | 44 | PF01217 | 0.560 |
TRG_DiLeu_BaLyEn_6 | 137 | 142 | PF01217 | 0.544 |
TRG_DiLeu_BaLyEn_6 | 207 | 212 | PF01217 | 0.640 |
TRG_DiLeu_LyEn_5 | 5 | 10 | PF01217 | 0.597 |
TRG_ENDOCYTIC_2 | 254 | 257 | PF00928 | 0.376 |
TRG_ER_diArg_1 | 333 | 336 | PF00400 | 0.517 |
TRG_ER_diArg_1 | 412 | 415 | PF00400 | 0.630 |
TRG_Pf-PMV_PEXEL_1 | 248 | 252 | PF00026 | 0.551 |
TRG_Pf-PMV_PEXEL_1 | 25 | 29 | PF00026 | 0.551 |
TRG_Pf-PMV_PEXEL_1 | 336 | 340 | PF00026 | 0.356 |
TRG_Pf-PMV_PEXEL_1 | 344 | 348 | PF00026 | 0.356 |
TRG_Pf-PMV_PEXEL_1 | 396 | 401 | PF00026 | 0.598 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4Y0 | Leptomonas seymouri | 42% | 100% |
A0A3S7WX61 | Leishmania donovani | 89% | 100% |
A4HCA5 | Leishmania braziliensis | 67% | 100% |
A4HZT7 | Leishmania infantum | 89% | 100% |
E9AVP2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |
V5BR45 | Trypanosoma cruzi | 33% | 100% |