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: 5 |
NetGPI | no | yes: 0, no: 5 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 1 |
GO:0016020 | membrane | 2 | 2 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: A4H4D6
Term | Name | Level | Count |
---|---|---|---|
GO:0000209 | protein polyubiquitination | 8 | 1 |
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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 4 |
GO:0016874 | ligase activity | 2 | 4 |
GO:0004842 | ubiquitin-protein transferase activity | 4 | 1 |
GO:0016740 | transferase activity | 2 | 1 |
GO:0019787 | ubiquitin-like protein transferase activity | 3 | 1 |
GO:0061631 | ubiquitin conjugating enzyme activity | 5 | 1 |
GO:0061650 | ubiquitin-like protein conjugating enzyme activity | 4 | 1 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 325 | 329 | PF00656 | 0.649 |
CLV_NRD_NRD_1 | 284 | 286 | PF00675 | 0.476 |
CLV_NRD_NRD_1 | 450 | 452 | PF00675 | 0.374 |
CLV_PCSK_KEX2_1 | 284 | 286 | PF00082 | 0.445 |
CLV_PCSK_KEX2_1 | 450 | 452 | PF00082 | 0.374 |
CLV_PCSK_KEX2_1 | 9 | 11 | PF00082 | 0.269 |
CLV_PCSK_PC1ET2_1 | 9 | 11 | PF00082 | 0.318 |
CLV_PCSK_PC7_1 | 280 | 286 | PF00082 | 0.443 |
CLV_PCSK_SKI1_1 | 334 | 338 | PF00082 | 0.470 |
CLV_PCSK_SKI1_1 | 416 | 420 | PF00082 | 0.500 |
DEG_APCC_DBOX_1 | 449 | 457 | PF00400 | 0.374 |
DEG_SCF_FBW7_1 | 212 | 219 | PF00400 | 0.660 |
DEG_SPOP_SBC_1 | 216 | 220 | PF00917 | 0.635 |
DOC_MAPK_MEF2A_6 | 135 | 142 | PF00069 | 0.491 |
DOC_MAPK_RevD_3 | 436 | 451 | PF00069 | 0.367 |
DOC_PP1_RVXF_1 | 449 | 456 | PF00149 | 0.231 |
DOC_PP2B_LxvP_1 | 249 | 252 | PF13499 | 0.737 |
DOC_PP2B_LxvP_1 | 73 | 76 | PF13499 | 0.518 |
DOC_SPAK_OSR1_1 | 86 | 90 | PF12202 | 0.469 |
DOC_USP7_MATH_1 | 216 | 220 | PF00917 | 0.696 |
DOC_USP7_MATH_1 | 301 | 305 | PF00917 | 0.687 |
DOC_WW_Pin1_4 | 174 | 179 | PF00397 | 0.646 |
DOC_WW_Pin1_4 | 212 | 217 | PF00397 | 0.699 |
DOC_WW_Pin1_4 | 241 | 246 | PF00397 | 0.736 |
DOC_WW_Pin1_4 | 250 | 255 | PF00397 | 0.664 |
DOC_WW_Pin1_4 | 259 | 264 | PF00397 | 0.618 |
DOC_WW_Pin1_4 | 279 | 284 | PF00397 | 0.683 |
DOC_WW_Pin1_4 | 303 | 308 | PF00397 | 0.758 |
DOC_WW_Pin1_4 | 314 | 319 | PF00397 | 0.687 |
DOC_WW_Pin1_4 | 348 | 353 | PF00397 | 0.718 |
DOC_WW_Pin1_4 | 362 | 367 | PF00397 | 0.677 |
DOC_WW_Pin1_4 | 394 | 399 | PF00397 | 0.709 |
LIG_Actin_RPEL_3 | 428 | 447 | PF02755 | 0.417 |
LIG_Actin_WH2_2 | 434 | 452 | PF00022 | 0.503 |
LIG_APCC_ABBA_1 | 170 | 175 | PF00400 | 0.605 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.555 |
LIG_BIR_III_4 | 342 | 346 | PF00653 | 0.627 |
LIG_BRCT_BRCA1_1 | 83 | 87 | PF00533 | 0.469 |
LIG_deltaCOP1_diTrp_1 | 144 | 153 | PF00928 | 0.569 |
LIG_deltaCOP1_diTrp_1 | 39 | 42 | PF00928 | 0.469 |
LIG_EVH1_2 | 264 | 268 | PF00568 | 0.643 |
LIG_FHA_1 | 106 | 112 | PF00498 | 0.518 |
LIG_FHA_1 | 160 | 166 | PF00498 | 0.552 |
LIG_FHA_1 | 304 | 310 | PF00498 | 0.735 |
LIG_FHA_1 | 394 | 400 | PF00498 | 0.719 |
LIG_FHA_2 | 159 | 165 | PF00498 | 0.507 |
LIG_FHA_2 | 377 | 383 | PF00498 | 0.660 |
LIG_GBD_Chelix_1 | 438 | 446 | PF00786 | 0.374 |
LIG_HCF-1_HBM_1 | 374 | 377 | PF13415 | 0.644 |
LIG_LIR_Apic_2 | 27 | 32 | PF02991 | 0.469 |
LIG_LIR_LC3C_4 | 440 | 445 | PF02991 | 0.231 |
LIG_LIR_Nem_3 | 12 | 18 | PF02991 | 0.518 |
LIG_LIR_Nem_3 | 266 | 271 | PF02991 | 0.649 |
LIG_LYPXL_S_1 | 172 | 176 | PF13949 | 0.304 |
LIG_LYPXL_yS_3 | 173 | 176 | PF13949 | 0.496 |
LIG_MYND_1 | 185 | 189 | PF01753 | 0.653 |
LIG_NRBOX | 452 | 458 | PF00104 | 0.451 |
LIG_Pex14_1 | 105 | 109 | PF04695 | 0.469 |
LIG_Pex14_2 | 38 | 42 | PF04695 | 0.469 |
LIG_REV1ctd_RIR_1 | 78 | 87 | PF16727 | 0.518 |
LIG_SH2_CRK | 29 | 33 | PF00017 | 0.433 |
LIG_SH2_SRC | 109 | 112 | PF00017 | 0.537 |
LIG_SH2_STAP1 | 109 | 113 | PF00017 | 0.469 |
LIG_SH2_STAP1 | 3 | 7 | PF00017 | 0.573 |
LIG_SH2_STAP1 | 377 | 381 | PF00017 | 0.679 |
LIG_SH2_STAT5 | 346 | 349 | PF00017 | 0.616 |
LIG_SH3_1 | 69 | 75 | PF00018 | 0.469 |
LIG_SH3_3 | 182 | 188 | PF00018 | 0.686 |
LIG_SH3_3 | 249 | 255 | PF00018 | 0.742 |
LIG_SH3_3 | 353 | 359 | PF00018 | 0.760 |
LIG_SH3_3 | 363 | 369 | PF00018 | 0.733 |
LIG_SH3_3 | 370 | 376 | PF00018 | 0.672 |
LIG_SH3_3 | 405 | 411 | PF00018 | 0.689 |
LIG_SH3_3 | 423 | 429 | PF00018 | 0.534 |
LIG_SH3_3 | 69 | 75 | PF00018 | 0.469 |
LIG_SUMO_SIM_anti_2 | 440 | 446 | PF11976 | 0.231 |
LIG_SUMO_SIM_par_1 | 136 | 141 | PF11976 | 0.547 |
LIG_TRFH_1 | 71 | 75 | PF08558 | 0.518 |
MOD_CDC14_SPxK_1 | 177 | 180 | PF00782 | 0.633 |
MOD_CDC14_SPxK_1 | 282 | 285 | PF00782 | 0.660 |
MOD_CDC14_SPxK_1 | 351 | 354 | PF00782 | 0.701 |
MOD_CDK_SPK_2 | 279 | 284 | PF00069 | 0.686 |
MOD_CDK_SPxK_1 | 174 | 180 | PF00069 | 0.623 |
MOD_CDK_SPxK_1 | 279 | 285 | PF00069 | 0.665 |
MOD_CDK_SPxK_1 | 348 | 354 | PF00069 | 0.705 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.627 |
MOD_CK1_1 | 214 | 220 | PF00069 | 0.711 |
MOD_CK1_1 | 225 | 231 | PF00069 | 0.631 |
MOD_CK1_1 | 250 | 256 | PF00069 | 0.643 |
MOD_CK1_1 | 279 | 285 | PF00069 | 0.654 |
MOD_CK1_1 | 330 | 336 | PF00069 | 0.801 |
MOD_CK1_1 | 397 | 403 | PF00069 | 0.655 |
MOD_CK1_1 | 95 | 101 | PF00069 | 0.483 |
MOD_CK2_1 | 376 | 382 | PF00069 | 0.623 |
MOD_GlcNHglycan | 196 | 199 | PF01048 | 0.573 |
MOD_GlcNHglycan | 249 | 252 | PF01048 | 0.444 |
MOD_GlcNHglycan | 276 | 279 | PF01048 | 0.450 |
MOD_GlcNHglycan | 328 | 332 | PF01048 | 0.637 |
MOD_GlcNHglycan | 83 | 86 | PF01048 | 0.287 |
MOD_GSK3_1 | 149 | 156 | PF00069 | 0.548 |
MOD_GSK3_1 | 190 | 197 | PF00069 | 0.678 |
MOD_GSK3_1 | 211 | 218 | PF00069 | 0.823 |
MOD_GSK3_1 | 225 | 232 | PF00069 | 0.660 |
MOD_GSK3_1 | 310 | 317 | PF00069 | 0.686 |
MOD_GSK3_1 | 376 | 383 | PF00069 | 0.675 |
MOD_GSK3_1 | 393 | 400 | PF00069 | 0.619 |
MOD_GSK3_1 | 92 | 99 | PF00069 | 0.478 |
MOD_LATS_1 | 90 | 96 | PF00433 | 0.417 |
MOD_NEK2_1 | 113 | 118 | PF00069 | 0.518 |
MOD_NEK2_1 | 153 | 158 | PF00069 | 0.584 |
MOD_NEK2_1 | 247 | 252 | PF00069 | 0.646 |
MOD_NEK2_1 | 271 | 276 | PF00069 | 0.651 |
MOD_NEK2_1 | 302 | 307 | PF00069 | 0.710 |
MOD_NEK2_1 | 361 | 366 | PF00069 | 0.634 |
MOD_NEK2_1 | 424 | 429 | PF00069 | 0.739 |
MOD_NEK2_1 | 65 | 70 | PF00069 | 0.572 |
MOD_NEK2_1 | 79 | 84 | PF00069 | 0.473 |
MOD_NEK2_2 | 40 | 45 | PF00069 | 0.518 |
MOD_PKA_1 | 9 | 15 | PF00069 | 0.518 |
MOD_PKA_2 | 9 | 15 | PF00069 | 0.553 |
MOD_Plk_1 | 310 | 316 | PF00069 | 0.659 |
MOD_Plk_1 | 424 | 430 | PF00069 | 0.678 |
MOD_Plk_1 | 50 | 56 | PF00069 | 0.557 |
MOD_Plk_4 | 218 | 224 | PF00069 | 0.675 |
MOD_Plk_4 | 380 | 386 | PF00069 | 0.699 |
MOD_Plk_4 | 437 | 443 | PF00069 | 0.309 |
MOD_ProDKin_1 | 174 | 180 | PF00069 | 0.646 |
MOD_ProDKin_1 | 212 | 218 | PF00069 | 0.698 |
MOD_ProDKin_1 | 241 | 247 | PF00069 | 0.737 |
MOD_ProDKin_1 | 250 | 256 | PF00069 | 0.663 |
MOD_ProDKin_1 | 259 | 265 | PF00069 | 0.617 |
MOD_ProDKin_1 | 279 | 285 | PF00069 | 0.694 |
MOD_ProDKin_1 | 303 | 309 | PF00069 | 0.760 |
MOD_ProDKin_1 | 314 | 320 | PF00069 | 0.687 |
MOD_ProDKin_1 | 348 | 354 | PF00069 | 0.719 |
MOD_ProDKin_1 | 362 | 368 | PF00069 | 0.676 |
MOD_ProDKin_1 | 394 | 400 | PF00069 | 0.713 |
MOD_SUMO_for_1 | 336 | 339 | PF00179 | 0.677 |
MOD_SUMO_rev_2 | 164 | 172 | PF00179 | 0.493 |
TRG_ENDOCYTIC_2 | 15 | 18 | PF00928 | 0.518 |
TRG_ENDOCYTIC_2 | 173 | 176 | PF00928 | 0.496 |
TRG_ER_diArg_1 | 283 | 285 | PF00400 | 0.636 |
TRG_ER_diArg_1 | 449 | 451 | PF00400 | 0.374 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S5H5K9 | Leishmania donovani | 59% | 99% |
A4HSL5 | Leishmania infantum | 59% | 98% |
Q4QJA9 | Leishmania major | 60% | 95% |
V5B702 | Trypanosoma cruzi | 39% | 100% |