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: 8 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005929 | cilium | 4 | 7 |
GO:0042995 | cell projection | 2 | 7 |
GO:0043226 | organelle | 2 | 7 |
GO:0043227 | membrane-bounded organelle | 3 | 7 |
GO:0110165 | cellular anatomical entity | 1 | 7 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 7 |
GO:0000151 | ubiquitin ligase complex | 3 | 1 |
GO:0005634 | nucleus | 5 | 1 |
GO:0005886 | plasma membrane | 3 | 1 |
GO:0016020 | membrane | 2 | 1 |
GO:0019005 | SCF ubiquitin ligase complex | 5 | 1 |
GO:0031461 | cullin-RING ubiquitin ligase complex | 4 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0140535 | intracellular protein-containing complex | 2 | 1 |
GO:1902494 | catalytic complex | 2 | 1 |
GO:1990234 | transferase complex | 3 | 1 |
Related structures:
AlphaFold database: A4H7D3
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 1 |
GO:0006511 | ubiquitin-dependent protein catabolic process | 7 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009056 | catabolic process | 2 | 1 |
GO:0009057 | macromolecule catabolic process | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0010498 | proteasomal protein catabolic process | 5 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0019941 | modification-dependent protein catabolic process | 6 | 1 |
GO:0030163 | protein catabolic process | 4 | 1 |
GO:0031146 | SCF-dependent proteasomal ubiquitin-dependent protein catabolic process | 7 | 1 |
GO:0043161 | proteasome-mediated ubiquitin-dependent protein catabolic process | 6 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043632 | modification-dependent macromolecule catabolic process | 5 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044248 | cellular catabolic process | 3 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
GO:0044265 | obsolete cellular macromolecule catabolic process | 4 | 1 |
GO:0051603 | proteolysis involved in protein catabolic process | 5 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
GO:1901565 | organonitrogen compound catabolic process | 4 | 1 |
GO:1901575 | organic substance catabolic process | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 573 | 575 | PF00675 | 0.485 |
CLV_PCSK_KEX2_1 | 502 | 504 | PF00082 | 0.440 |
CLV_PCSK_KEX2_1 | 575 | 577 | PF00082 | 0.347 |
CLV_PCSK_PC1ET2_1 | 502 | 504 | PF00082 | 0.440 |
CLV_PCSK_PC1ET2_1 | 575 | 577 | PF00082 | 0.347 |
CLV_PCSK_SKI1_1 | 26 | 30 | PF00082 | 0.584 |
CLV_PCSK_SKI1_1 | 287 | 291 | PF00082 | 0.413 |
CLV_PCSK_SKI1_1 | 502 | 506 | PF00082 | 0.420 |
CLV_PCSK_SKI1_1 | 553 | 557 | PF00082 | 0.379 |
DEG_APCC_DBOX_1 | 575 | 583 | PF00400 | 0.335 |
DEG_SCF_FBW7_1 | 84 | 89 | PF00400 | 0.551 |
DOC_CDC14_PxL_1 | 545 | 553 | PF14671 | 0.389 |
DOC_CKS1_1 | 63 | 68 | PF01111 | 0.523 |
DOC_CYCLIN_RxL_1 | 434 | 442 | PF00134 | 0.380 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 351 | 360 | PF00134 | 0.259 |
DOC_CYCLIN_yCln2_LP_2 | 63 | 69 | PF00134 | 0.505 |
DOC_MAPK_gen_1 | 502 | 509 | PF00069 | 0.388 |
DOC_MAPK_gen_1 | 574 | 583 | PF00069 | 0.417 |
DOC_MAPK_MEF2A_6 | 574 | 583 | PF00069 | 0.330 |
DOC_PP1_RVXF_1 | 460 | 467 | PF00149 | 0.441 |
DOC_PP2B_LxvP_1 | 468 | 471 | PF13499 | 0.469 |
DOC_PP4_FxxP_1 | 583 | 586 | PF00568 | 0.377 |
DOC_USP7_MATH_1 | 111 | 115 | PF00917 | 0.569 |
DOC_USP7_MATH_1 | 181 | 185 | PF00917 | 0.532 |
DOC_USP7_MATH_1 | 189 | 193 | PF00917 | 0.545 |
DOC_USP7_MATH_1 | 246 | 250 | PF00917 | 0.664 |
DOC_USP7_MATH_1 | 261 | 265 | PF00917 | 0.389 |
DOC_USP7_MATH_1 | 380 | 384 | PF00917 | 0.331 |
DOC_USP7_MATH_1 | 79 | 83 | PF00917 | 0.735 |
DOC_WW_Pin1_4 | 100 | 105 | PF00397 | 0.620 |
DOC_WW_Pin1_4 | 145 | 150 | PF00397 | 0.632 |
DOC_WW_Pin1_4 | 165 | 170 | PF00397 | 0.608 |
DOC_WW_Pin1_4 | 213 | 218 | PF00397 | 0.622 |
DOC_WW_Pin1_4 | 307 | 312 | PF00397 | 0.543 |
DOC_WW_Pin1_4 | 599 | 604 | PF00397 | 0.631 |
DOC_WW_Pin1_4 | 612 | 617 | PF00397 | 0.593 |
DOC_WW_Pin1_4 | 62 | 67 | PF00397 | 0.588 |
DOC_WW_Pin1_4 | 75 | 80 | PF00397 | 0.660 |
DOC_WW_Pin1_4 | 82 | 87 | PF00397 | 0.634 |
LIG_14-3-3_CanoR_1 | 319 | 328 | PF00244 | 0.553 |
LIG_14-3-3_CanoR_1 | 338 | 345 | PF00244 | 0.312 |
LIG_14-3-3_CanoR_1 | 405 | 412 | PF00244 | 0.367 |
LIG_14-3-3_CanoR_1 | 503 | 508 | PF00244 | 0.408 |
LIG_14-3-3_CanoR_1 | 521 | 525 | PF00244 | 0.379 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.571 |
LIG_BIR_III_1 | 1 | 5 | PF00653 | 0.647 |
LIG_BIR_III_2 | 341 | 345 | PF00653 | 0.336 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.647 |
LIG_BRCT_BRCA1_1 | 191 | 195 | PF00533 | 0.538 |
LIG_BRCT_BRCA1_1 | 348 | 352 | PF00533 | 0.392 |
LIG_FHA_1 | 155 | 161 | PF00498 | 0.691 |
LIG_FHA_1 | 168 | 174 | PF00498 | 0.576 |
LIG_FHA_1 | 23 | 29 | PF00498 | 0.604 |
LIG_FHA_1 | 264 | 270 | PF00498 | 0.368 |
LIG_FHA_1 | 361 | 367 | PF00498 | 0.520 |
LIG_FHA_1 | 426 | 432 | PF00498 | 0.346 |
LIG_FHA_1 | 504 | 510 | PF00498 | 0.411 |
LIG_FHA_1 | 528 | 534 | PF00498 | 0.261 |
LIG_FHA_1 | 550 | 556 | PF00498 | 0.499 |
LIG_FHA_1 | 79 | 85 | PF00498 | 0.670 |
LIG_FHA_2 | 145 | 151 | PF00498 | 0.688 |
LIG_FHA_2 | 538 | 544 | PF00498 | 0.376 |
LIG_FHA_2 | 616 | 622 | PF00498 | 0.672 |
LIG_LIR_Apic_2 | 580 | 586 | PF02991 | 0.375 |
LIG_LIR_Nem_3 | 174 | 179 | PF02991 | 0.676 |
LIG_LIR_Nem_3 | 65 | 70 | PF02991 | 0.604 |
LIG_LYPXL_yS_3 | 70 | 73 | PF13949 | 0.598 |
LIG_NRBOX | 463 | 469 | PF00104 | 0.440 |
LIG_Rb_pABgroove_1 | 346 | 354 | PF01858 | 0.361 |
LIG_SH2_STAP1 | 406 | 410 | PF00017 | 0.365 |
LIG_SH2_STAT3 | 99 | 102 | PF00017 | 0.689 |
LIG_SH2_STAT5 | 403 | 406 | PF00017 | 0.348 |
LIG_SH3_1 | 101 | 107 | PF00018 | 0.681 |
LIG_SH3_1 | 606 | 612 | PF00018 | 0.668 |
LIG_SH3_3 | 101 | 107 | PF00018 | 0.677 |
LIG_SH3_3 | 180 | 186 | PF00018 | 0.577 |
LIG_SH3_3 | 188 | 194 | PF00018 | 0.738 |
LIG_SH3_3 | 207 | 213 | PF00018 | 0.644 |
LIG_SH3_3 | 606 | 612 | PF00018 | 0.668 |
LIG_SH3_3 | 85 | 91 | PF00018 | 0.818 |
LIG_SUMO_SIM_par_1 | 481 | 486 | PF11976 | 0.341 |
LIG_UBA3_1 | 467 | 475 | PF00899 | 0.332 |
LIG_WRC_WIRS_1 | 491 | 496 | PF05994 | 0.424 |
MOD_CDC14_SPxK_1 | 216 | 219 | PF00782 | 0.522 |
MOD_CDK_SPxK_1 | 213 | 219 | PF00069 | 0.524 |
MOD_CDK_SPxxK_3 | 599 | 606 | PF00069 | 0.644 |
MOD_CK1_1 | 120 | 126 | PF00069 | 0.588 |
MOD_CK1_1 | 168 | 174 | PF00069 | 0.601 |
MOD_CK1_1 | 215 | 221 | PF00069 | 0.594 |
MOD_CK1_1 | 232 | 238 | PF00069 | 0.641 |
MOD_CK1_1 | 388 | 394 | PF00069 | 0.329 |
MOD_CK1_1 | 490 | 496 | PF00069 | 0.374 |
MOD_CK1_1 | 610 | 616 | PF00069 | 0.648 |
MOD_CK1_1 | 78 | 84 | PF00069 | 0.707 |
MOD_CK2_1 | 144 | 150 | PF00069 | 0.685 |
MOD_CK2_1 | 261 | 267 | PF00069 | 0.456 |
MOD_CK2_1 | 537 | 543 | PF00069 | 0.339 |
MOD_CK2_1 | 615 | 621 | PF00069 | 0.672 |
MOD_GlcNHglycan | 114 | 117 | PF01048 | 0.663 |
MOD_GlcNHglycan | 170 | 173 | PF01048 | 0.669 |
MOD_GlcNHglycan | 244 | 247 | PF01048 | 0.489 |
MOD_GlcNHglycan | 314 | 318 | PF01048 | 0.396 |
MOD_GlcNHglycan | 356 | 359 | PF01048 | 0.338 |
MOD_GlcNHglycan | 525 | 528 | PF01048 | 0.362 |
MOD_GlcNHglycan | 54 | 57 | PF01048 | 0.545 |
MOD_GlcNHglycan | 593 | 596 | PF01048 | 0.706 |
MOD_GSK3_1 | 156 | 163 | PF00069 | 0.615 |
MOD_GSK3_1 | 167 | 174 | PF00069 | 0.637 |
MOD_GSK3_1 | 200 | 207 | PF00069 | 0.615 |
MOD_GSK3_1 | 242 | 249 | PF00069 | 0.570 |
MOD_GSK3_1 | 251 | 258 | PF00069 | 0.482 |
MOD_GSK3_1 | 261 | 268 | PF00069 | 0.508 |
MOD_GSK3_1 | 269 | 276 | PF00069 | 0.408 |
MOD_GSK3_1 | 356 | 363 | PF00069 | 0.377 |
MOD_GSK3_1 | 385 | 392 | PF00069 | 0.336 |
MOD_GSK3_1 | 493 | 500 | PF00069 | 0.348 |
MOD_GSK3_1 | 503 | 510 | PF00069 | 0.427 |
MOD_GSK3_1 | 523 | 530 | PF00069 | 0.300 |
MOD_GSK3_1 | 58 | 65 | PF00069 | 0.530 |
MOD_GSK3_1 | 597 | 604 | PF00069 | 0.626 |
MOD_GSK3_1 | 71 | 78 | PF00069 | 0.728 |
MOD_GSK3_1 | 82 | 89 | PF00069 | 0.603 |
MOD_N-GLC_1 | 112 | 117 | PF02516 | 0.555 |
MOD_N-GLC_1 | 145 | 150 | PF02516 | 0.529 |
MOD_N-GLC_1 | 246 | 251 | PF02516 | 0.614 |
MOD_N-GLC_1 | 33 | 38 | PF02516 | 0.655 |
MOD_N-GLC_1 | 354 | 359 | PF02516 | 0.330 |
MOD_N-GLC_1 | 394 | 399 | PF02516 | 0.473 |
MOD_N-GLC_1 | 82 | 87 | PF02516 | 0.710 |
MOD_N-GLC_2 | 332 | 334 | PF02516 | 0.423 |
MOD_N-GLC_2 | 382 | 384 | PF02516 | 0.336 |
MOD_NEK2_1 | 160 | 165 | PF00069 | 0.569 |
MOD_NEK2_1 | 22 | 27 | PF00069 | 0.501 |
MOD_NEK2_1 | 231 | 236 | PF00069 | 0.588 |
MOD_NEK2_1 | 251 | 256 | PF00069 | 0.493 |
MOD_NEK2_1 | 269 | 274 | PF00069 | 0.413 |
MOD_NEK2_1 | 320 | 325 | PF00069 | 0.368 |
MOD_NEK2_1 | 354 | 359 | PF00069 | 0.363 |
MOD_NEK2_1 | 360 | 365 | PF00069 | 0.496 |
MOD_NEK2_1 | 439 | 444 | PF00069 | 0.510 |
MOD_NEK2_1 | 507 | 512 | PF00069 | 0.338 |
MOD_NEK2_1 | 59 | 64 | PF00069 | 0.531 |
MOD_NEK2_2 | 527 | 532 | PF00069 | 0.267 |
MOD_PIKK_1 | 456 | 462 | PF00454 | 0.370 |
MOD_PKA_2 | 326 | 332 | PF00069 | 0.397 |
MOD_PKA_2 | 337 | 343 | PF00069 | 0.396 |
MOD_PKA_2 | 404 | 410 | PF00069 | 0.358 |
MOD_PKA_2 | 507 | 513 | PF00069 | 0.374 |
MOD_PKA_2 | 520 | 526 | PF00069 | 0.387 |
MOD_Plk_1 | 112 | 118 | PF00069 | 0.551 |
MOD_Plk_1 | 200 | 206 | PF00069 | 0.574 |
MOD_Plk_1 | 232 | 238 | PF00069 | 0.548 |
MOD_Plk_1 | 246 | 252 | PF00069 | 0.554 |
MOD_Plk_1 | 313 | 319 | PF00069 | 0.311 |
MOD_Plk_1 | 33 | 39 | PF00069 | 0.657 |
MOD_Plk_1 | 388 | 394 | PF00069 | 0.368 |
MOD_Plk_1 | 439 | 445 | PF00069 | 0.350 |
MOD_Plk_1 | 456 | 462 | PF00069 | 0.370 |
MOD_Plk_4 | 156 | 162 | PF00069 | 0.734 |
MOD_Plk_4 | 204 | 210 | PF00069 | 0.674 |
MOD_Plk_4 | 346 | 352 | PF00069 | 0.396 |
MOD_Plk_4 | 356 | 362 | PF00069 | 0.478 |
MOD_Plk_4 | 414 | 420 | PF00069 | 0.377 |
MOD_Plk_4 | 487 | 493 | PF00069 | 0.325 |
MOD_Plk_4 | 94 | 100 | PF00069 | 0.525 |
MOD_ProDKin_1 | 100 | 106 | PF00069 | 0.620 |
MOD_ProDKin_1 | 145 | 151 | PF00069 | 0.634 |
MOD_ProDKin_1 | 165 | 171 | PF00069 | 0.608 |
MOD_ProDKin_1 | 213 | 219 | PF00069 | 0.622 |
MOD_ProDKin_1 | 307 | 313 | PF00069 | 0.538 |
MOD_ProDKin_1 | 599 | 605 | PF00069 | 0.630 |
MOD_ProDKin_1 | 612 | 618 | PF00069 | 0.596 |
MOD_ProDKin_1 | 62 | 68 | PF00069 | 0.591 |
MOD_ProDKin_1 | 75 | 81 | PF00069 | 0.663 |
MOD_ProDKin_1 | 82 | 88 | PF00069 | 0.632 |
MOD_SUMO_rev_2 | 114 | 123 | PF00179 | 0.662 |
MOD_SUMO_rev_2 | 392 | 402 | PF00179 | 0.355 |
TRG_ENDOCYTIC_2 | 70 | 73 | PF00928 | 0.598 |
TRG_ER_diArg_1 | 573 | 576 | PF00400 | 0.321 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5N0 | Leptomonas seymouri | 63% | 100% |
A0A3S7X7J0 | Leishmania donovani | 82% | 100% |
A4I9M5 | Leishmania infantum | 82% | 100% |
E9B4M4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 100% |
Q4Q3F2 | Leishmania major | 82% | 100% |