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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000151 | ubiquitin ligase complex | 3 | 1 |
GO:0031461 | cullin-RING ubiquitin ligase complex | 4 | 1 |
GO:0031464 | Cul4A-RING E3 ubiquitin ligase complex | 6 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0080008 | Cul4-RING E3 ubiquitin ligase complex | 5 | 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: A4HTX8
Term | Name | Level | Count |
---|---|---|---|
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0016567 | protein ubiquitination | 7 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0032446 | protein modification by small protein conjugation | 6 | 1 |
GO:0036211 | protein modification process | 4 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0070647 | protein modification by small protein conjugation or removal | 5 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 123 | 127 | PF00656 | 0.583 |
CLV_C14_Caspase3-7 | 315 | 319 | PF00656 | 0.709 |
CLV_C14_Caspase3-7 | 427 | 431 | PF00656 | 0.529 |
CLV_NRD_NRD_1 | 211 | 213 | PF00675 | 0.543 |
CLV_NRD_NRD_1 | 231 | 233 | PF00675 | 0.483 |
CLV_NRD_NRD_1 | 242 | 244 | PF00675 | 0.507 |
CLV_NRD_NRD_1 | 379 | 381 | PF00675 | 0.405 |
CLV_NRD_NRD_1 | 388 | 390 | PF00675 | 0.417 |
CLV_NRD_NRD_1 | 79 | 81 | PF00675 | 0.416 |
CLV_PCSK_FUR_1 | 376 | 380 | PF00082 | 0.420 |
CLV_PCSK_KEX2_1 | 211 | 213 | PF00082 | 0.543 |
CLV_PCSK_KEX2_1 | 378 | 380 | PF00082 | 0.412 |
CLV_PCSK_KEX2_1 | 381 | 383 | PF00082 | 0.407 |
CLV_PCSK_KEX2_1 | 388 | 390 | PF00082 | 0.409 |
CLV_PCSK_KEX2_1 | 79 | 81 | PF00082 | 0.420 |
CLV_PCSK_PC1ET2_1 | 381 | 383 | PF00082 | 0.412 |
DEG_APCC_DBOX_1 | 79 | 87 | PF00400 | 0.393 |
DEG_SCF_FBW7_2 | 94 | 101 | PF00400 | 0.573 |
DEG_SPOP_SBC_1 | 115 | 119 | PF00917 | 0.535 |
DEG_SPOP_SBC_1 | 155 | 159 | PF00917 | 0.528 |
DEG_SPOP_SBC_1 | 261 | 265 | PF00917 | 0.691 |
DEG_SPOP_SBC_1 | 5 | 9 | PF00917 | 0.555 |
DOC_ANK_TNKS_1 | 279 | 286 | PF00023 | 0.654 |
DOC_CDC14_PxL_1 | 417 | 425 | PF14671 | 0.467 |
DOC_MAPK_gen_1 | 388 | 394 | PF00069 | 0.435 |
DOC_MAPK_gen_1 | 79 | 86 | PF00069 | 0.378 |
DOC_MAPK_MEF2A_6 | 85 | 94 | PF00069 | 0.432 |
DOC_MIT_MIM_1 | 384 | 393 | PF04212 | 0.383 |
DOC_PP1_RVXF_1 | 366 | 373 | PF00149 | 0.500 |
DOC_PP2B_LxvP_1 | 160 | 163 | PF13499 | 0.495 |
DOC_PP2B_LxvP_1 | 297 | 300 | PF13499 | 0.700 |
DOC_PP2B_LxvP_1 | 392 | 395 | PF13499 | 0.438 |
DOC_USP7_MATH_1 | 109 | 113 | PF00917 | 0.616 |
DOC_USP7_MATH_1 | 11 | 15 | PF00917 | 0.574 |
DOC_USP7_MATH_1 | 115 | 119 | PF00917 | 0.562 |
DOC_USP7_MATH_1 | 255 | 259 | PF00917 | 0.710 |
DOC_USP7_MATH_1 | 260 | 264 | PF00917 | 0.824 |
DOC_USP7_MATH_1 | 292 | 296 | PF00917 | 0.693 |
DOC_USP7_MATH_1 | 3 | 7 | PF00917 | 0.624 |
DOC_USP7_MATH_1 | 300 | 304 | PF00917 | 0.601 |
DOC_USP7_MATH_1 | 32 | 36 | PF00917 | 0.352 |
DOC_USP7_MATH_1 | 362 | 366 | PF00917 | 0.422 |
DOC_WW_Pin1_4 | 1 | 6 | PF00397 | 0.772 |
DOC_WW_Pin1_4 | 13 | 18 | PF00397 | 0.567 |
DOC_WW_Pin1_4 | 262 | 267 | PF00397 | 0.621 |
DOC_WW_Pin1_4 | 341 | 346 | PF00397 | 0.445 |
DOC_WW_Pin1_4 | 62 | 67 | PF00397 | 0.473 |
DOC_WW_Pin1_4 | 94 | 99 | PF00397 | 0.653 |
LIG_14-3-3_CanoR_1 | 153 | 163 | PF00244 | 0.516 |
LIG_14-3-3_CanoR_1 | 293 | 300 | PF00244 | 0.618 |
LIG_14-3-3_CanoR_1 | 388 | 393 | PF00244 | 0.441 |
LIG_14-3-3_CanoR_1 | 93 | 98 | PF00244 | 0.650 |
LIG_Actin_WH2_2 | 77 | 95 | PF00022 | 0.361 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.666 |
LIG_BIR_III_4 | 148 | 152 | PF00653 | 0.668 |
LIG_BRCT_BRCA1_1 | 428 | 432 | PF00533 | 0.508 |
LIG_EH1_1 | 360 | 368 | PF00400 | 0.499 |
LIG_EH1_1 | 410 | 418 | PF00400 | 0.454 |
LIG_eIF4E_1 | 361 | 367 | PF01652 | 0.419 |
LIG_FHA_1 | 18 | 24 | PF00498 | 0.426 |
LIG_FHA_1 | 385 | 391 | PF00498 | 0.481 |
LIG_FHA_1 | 435 | 441 | PF00498 | 0.465 |
LIG_FHA_1 | 89 | 95 | PF00498 | 0.413 |
LIG_FHA_2 | 313 | 319 | PF00498 | 0.708 |
LIG_LIR_Gen_1 | 35 | 45 | PF02991 | 0.412 |
LIG_LIR_Gen_1 | 409 | 418 | PF02991 | 0.448 |
LIG_LIR_Nem_3 | 178 | 183 | PF02991 | 0.409 |
LIG_LIR_Nem_3 | 344 | 350 | PF02991 | 0.403 |
LIG_LIR_Nem_3 | 35 | 40 | PF02991 | 0.368 |
LIG_LIR_Nem_3 | 405 | 410 | PF02991 | 0.476 |
LIG_PTAP_UEV_1 | 269 | 274 | PF05743 | 0.658 |
LIG_SH2_CRK | 418 | 422 | PF00017 | 0.476 |
LIG_SH2_STAP1 | 183 | 187 | PF00017 | 0.343 |
LIG_SH2_STAP1 | 54 | 58 | PF00017 | 0.429 |
LIG_SH3_1 | 418 | 424 | PF00018 | 0.525 |
LIG_SH3_3 | 264 | 270 | PF00018 | 0.658 |
LIG_SH3_3 | 356 | 362 | PF00018 | 0.488 |
LIG_SH3_3 | 418 | 424 | PF00018 | 0.525 |
LIG_SUMO_SIM_anti_2 | 20 | 25 | PF11976 | 0.403 |
LIG_TRAF2_1 | 236 | 239 | PF00917 | 0.646 |
LIG_TRAF2_1 | 41 | 44 | PF00917 | 0.461 |
LIG_TRAF2_1 | 424 | 427 | PF00917 | 0.496 |
MOD_CK1_1 | 303 | 309 | PF00069 | 0.632 |
MOD_CK1_1 | 312 | 318 | PF00069 | 0.592 |
MOD_CK1_1 | 4 | 10 | PF00069 | 0.774 |
MOD_CK1_1 | 473 | 479 | PF00069 | 0.633 |
MOD_CK1_1 | 96 | 102 | PF00069 | 0.598 |
MOD_CK2_1 | 161 | 167 | PF00069 | 0.477 |
MOD_CK2_1 | 303 | 309 | PF00069 | 0.603 |
MOD_CK2_1 | 478 | 484 | PF00069 | 0.679 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.639 |
MOD_GlcNHglycan | 13 | 16 | PF01048 | 0.537 |
MOD_GlcNHglycan | 218 | 221 | PF01048 | 0.635 |
MOD_GlcNHglycan | 270 | 273 | PF01048 | 0.694 |
MOD_GlcNHglycan | 289 | 292 | PF01048 | 0.632 |
MOD_GlcNHglycan | 323 | 328 | PF01048 | 0.654 |
MOD_GlcNHglycan | 472 | 475 | PF01048 | 0.600 |
MOD_GlcNHglycan | 480 | 483 | PF01048 | 0.562 |
MOD_GlcNHglycan | 71 | 74 | PF01048 | 0.411 |
MOD_GlcNHglycan | 76 | 79 | PF01048 | 0.467 |
MOD_GlcNHglycan | 98 | 101 | PF01048 | 0.602 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.614 |
MOD_GSK3_1 | 116 | 123 | PF00069 | 0.557 |
MOD_GSK3_1 | 13 | 20 | PF00069 | 0.515 |
MOD_GSK3_1 | 167 | 174 | PF00069 | 0.522 |
MOD_GSK3_1 | 216 | 223 | PF00069 | 0.651 |
MOD_GSK3_1 | 244 | 251 | PF00069 | 0.597 |
MOD_GSK3_1 | 300 | 307 | PF00069 | 0.660 |
MOD_GSK3_1 | 308 | 315 | PF00069 | 0.628 |
MOD_GSK3_1 | 384 | 391 | PF00069 | 0.432 |
MOD_GSK3_1 | 434 | 441 | PF00069 | 0.452 |
MOD_GSK3_1 | 466 | 473 | PF00069 | 0.517 |
MOD_N-GLC_1 | 168 | 173 | PF02516 | 0.370 |
MOD_N-GLC_1 | 188 | 193 | PF02516 | 0.259 |
MOD_N-GLC_1 | 470 | 475 | PF02516 | 0.556 |
MOD_N-GLC_1 | 62 | 67 | PF02516 | 0.451 |
MOD_NEK2_1 | 397 | 402 | PF00069 | 0.452 |
MOD_NEK2_2 | 156 | 161 | PF00069 | 0.544 |
MOD_NEK2_2 | 168 | 173 | PF00069 | 0.350 |
MOD_NEK2_2 | 88 | 93 | PF00069 | 0.407 |
MOD_PIKK_1 | 255 | 261 | PF00454 | 0.637 |
MOD_PKA_1 | 388 | 394 | PF00069 | 0.435 |
MOD_PKA_2 | 214 | 220 | PF00069 | 0.736 |
MOD_PKA_2 | 292 | 298 | PF00069 | 0.622 |
MOD_PKA_2 | 388 | 394 | PF00069 | 0.463 |
MOD_PKA_2 | 397 | 403 | PF00069 | 0.546 |
MOD_Plk_1 | 168 | 174 | PF00069 | 0.413 |
MOD_Plk_1 | 175 | 181 | PF00069 | 0.371 |
MOD_Plk_1 | 323 | 329 | PF00069 | 0.623 |
MOD_Plk_2-3 | 304 | 310 | PF00069 | 0.690 |
MOD_Plk_4 | 120 | 126 | PF00069 | 0.587 |
MOD_Plk_4 | 161 | 167 | PF00069 | 0.508 |
MOD_Plk_4 | 168 | 174 | PF00069 | 0.401 |
MOD_Plk_4 | 175 | 181 | PF00069 | 0.334 |
MOD_Plk_4 | 32 | 38 | PF00069 | 0.407 |
MOD_Plk_4 | 362 | 368 | PF00069 | 0.428 |
MOD_Plk_4 | 388 | 394 | PF00069 | 0.385 |
MOD_ProDKin_1 | 1 | 7 | PF00069 | 0.772 |
MOD_ProDKin_1 | 13 | 19 | PF00069 | 0.549 |
MOD_ProDKin_1 | 262 | 268 | PF00069 | 0.621 |
MOD_ProDKin_1 | 341 | 347 | PF00069 | 0.436 |
MOD_ProDKin_1 | 62 | 68 | PF00069 | 0.463 |
MOD_ProDKin_1 | 94 | 100 | PF00069 | 0.658 |
TRG_DiLeu_BaLyEn_6 | 418 | 423 | PF01217 | 0.464 |
TRG_ENDOCYTIC_2 | 410 | 413 | PF00928 | 0.442 |
TRG_ER_diArg_1 | 211 | 213 | PF00400 | 0.549 |
TRG_ER_diArg_1 | 376 | 379 | PF00400 | 0.425 |
TRG_ER_diArg_1 | 380 | 383 | PF00400 | 0.392 |
TRG_ER_diArg_1 | 388 | 390 | PF00400 | 0.392 |
TRG_ER_diArg_1 | 79 | 81 | PF00400 | 0.416 |
TRG_NLS_MonoExtN_4 | 230 | 236 | PF00514 | 0.642 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5U2 | Leptomonas seymouri | 40% | 100% |
A0A3S7WQQ0 | Leishmania donovani | 100% | 100% |
A4H5N4 | Leishmania braziliensis | 71% | 100% |
E9AMQ8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
Q4QHW7 | Leishmania major | 91% | 100% |