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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000776 | kinetochore | 3 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:0099080 | supramolecular complex | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4I780
Term | Name | Level | Count |
---|---|---|---|
GO:0007059 | chromosome segregation | 2 | 1 |
GO:0009987 | cellular process | 1 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 418 | 422 | PF00656 | 0.617 |
CLV_NRD_NRD_1 | 186 | 188 | PF00675 | 0.559 |
CLV_NRD_NRD_1 | 19 | 21 | PF00675 | 0.595 |
CLV_NRD_NRD_1 | 269 | 271 | PF00675 | 0.494 |
CLV_NRD_NRD_1 | 282 | 284 | PF00675 | 0.338 |
CLV_NRD_NRD_1 | 307 | 309 | PF00675 | 0.544 |
CLV_NRD_NRD_1 | 337 | 339 | PF00675 | 0.733 |
CLV_NRD_NRD_1 | 426 | 428 | PF00675 | 0.690 |
CLV_PCSK_FUR_1 | 280 | 284 | PF00082 | 0.523 |
CLV_PCSK_KEX2_1 | 19 | 21 | PF00082 | 0.566 |
CLV_PCSK_KEX2_1 | 268 | 270 | PF00082 | 0.490 |
CLV_PCSK_KEX2_1 | 280 | 282 | PF00082 | 0.338 |
CLV_PCSK_KEX2_1 | 298 | 300 | PF00082 | 0.528 |
CLV_PCSK_KEX2_1 | 337 | 339 | PF00082 | 0.750 |
CLV_PCSK_KEX2_1 | 425 | 427 | PF00082 | 0.555 |
CLV_PCSK_PC1ET2_1 | 298 | 300 | PF00082 | 0.411 |
CLV_PCSK_PC1ET2_1 | 425 | 427 | PF00082 | 0.555 |
CLV_PCSK_SKI1_1 | 315 | 319 | PF00082 | 0.508 |
CLV_PCSK_SKI1_1 | 342 | 346 | PF00082 | 0.557 |
DEG_APCC_DBOX_1 | 176 | 184 | PF00400 | 0.490 |
DEG_APCC_DBOX_1 | 319 | 327 | PF00400 | 0.613 |
DEG_APCC_DBOX_1 | 76 | 84 | PF00400 | 0.522 |
DEG_SPOP_SBC_1 | 42 | 46 | PF00917 | 0.651 |
DEG_SPOP_SBC_1 | 83 | 87 | PF00917 | 0.531 |
DOC_MAPK_gen_1 | 177 | 185 | PF00069 | 0.456 |
DOC_MAPK_gen_1 | 288 | 297 | PF00069 | 0.570 |
DOC_MAPK_gen_1 | 425 | 431 | PF00069 | 0.560 |
DOC_MAPK_MEF2A_6 | 210 | 219 | PF00069 | 0.492 |
DOC_PP1_RVXF_1 | 340 | 347 | PF00149 | 0.542 |
DOC_PP2B_LxvP_1 | 39 | 42 | PF13499 | 0.574 |
DOC_USP7_MATH_1 | 161 | 165 | PF00917 | 0.407 |
DOC_USP7_MATH_1 | 348 | 352 | PF00917 | 0.576 |
DOC_USP7_MATH_1 | 42 | 46 | PF00917 | 0.668 |
DOC_USP7_MATH_1 | 65 | 69 | PF00917 | 0.648 |
DOC_USP7_MATH_1 | 8 | 12 | PF00917 | 0.672 |
DOC_USP7_UBL2_3 | 305 | 309 | PF12436 | 0.506 |
DOC_WW_Pin1_4 | 10 | 15 | PF00397 | 0.539 |
DOC_WW_Pin1_4 | 92 | 97 | PF00397 | 0.677 |
LIG_14-3-3_CanoR_1 | 10 | 14 | PF00244 | 0.539 |
LIG_14-3-3_CanoR_1 | 141 | 145 | PF00244 | 0.607 |
LIG_14-3-3_CanoR_1 | 210 | 215 | PF00244 | 0.523 |
LIG_14-3-3_CanoR_1 | 337 | 344 | PF00244 | 0.587 |
LIG_14-3-3_CanoR_1 | 40 | 48 | PF00244 | 0.637 |
LIG_14-3-3_CanoR_1 | 66 | 72 | PF00244 | 0.668 |
LIG_14-3-3_CanoR_1 | 77 | 81 | PF00244 | 0.615 |
LIG_14-3-3_CanoR_1 | 82 | 92 | PF00244 | 0.582 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.682 |
LIG_BRCT_BRCA1_1 | 410 | 414 | PF00533 | 0.671 |
LIG_CaM_IQ_9 | 180 | 196 | PF13499 | 0.543 |
LIG_FHA_1 | 11 | 17 | PF00498 | 0.537 |
LIG_FHA_1 | 211 | 217 | PF00498 | 0.484 |
LIG_FHA_1 | 252 | 258 | PF00498 | 0.560 |
LIG_FHA_2 | 367 | 373 | PF00498 | 0.741 |
LIG_GSK3_LRP6_1 | 92 | 97 | PF00069 | 0.572 |
LIG_IBAR_NPY_1 | 108 | 110 | PF08397 | 0.652 |
LIG_LIR_Apic_2 | 143 | 147 | PF02991 | 0.611 |
LIG_LIR_Apic_2 | 209 | 215 | PF02991 | 0.454 |
LIG_LIR_Apic_2 | 27 | 32 | PF02991 | 0.622 |
LIG_LIR_Apic_2 | 63 | 67 | PF02991 | 0.736 |
LIG_LIR_Apic_2 | 99 | 104 | PF02991 | 0.666 |
LIG_LIR_Gen_1 | 198 | 205 | PF02991 | 0.410 |
LIG_LIR_Gen_1 | 273 | 279 | PF02991 | 0.414 |
LIG_LIR_Nem_3 | 27 | 31 | PF02991 | 0.623 |
LIG_LIR_Nem_3 | 273 | 278 | PF02991 | 0.401 |
LIG_LIR_Nem_3 | 290 | 295 | PF02991 | 0.400 |
LIG_LIR_Nem_3 | 396 | 402 | PF02991 | 0.739 |
LIG_LYPXL_yS_3 | 149 | 152 | PF13949 | 0.651 |
LIG_MYND_1 | 150 | 154 | PF01753 | 0.567 |
LIG_SH2_CRK | 144 | 148 | PF00017 | 0.569 |
LIG_SH2_CRK | 29 | 33 | PF00017 | 0.690 |
LIG_SH2_CRK | 6 | 10 | PF00017 | 0.620 |
LIG_SH2_NCK_1 | 29 | 33 | PF00017 | 0.690 |
LIG_SH2_PTP2 | 101 | 104 | PF00017 | 0.558 |
LIG_SH2_STAT3 | 132 | 135 | PF00017 | 0.630 |
LIG_SH2_STAT5 | 101 | 104 | PF00017 | 0.696 |
LIG_SH2_STAT5 | 132 | 135 | PF00017 | 0.570 |
LIG_SH2_STAT5 | 196 | 199 | PF00017 | 0.522 |
LIG_SH2_STAT5 | 212 | 215 | PF00017 | 0.432 |
LIG_SH2_STAT5 | 256 | 259 | PF00017 | 0.552 |
LIG_SH2_STAT5 | 29 | 32 | PF00017 | 0.576 |
LIG_SH2_STAT5 | 292 | 295 | PF00017 | 0.528 |
LIG_SH2_STAT5 | 381 | 384 | PF00017 | 0.645 |
LIG_SH3_1 | 144 | 150 | PF00018 | 0.482 |
LIG_SH3_3 | 103 | 109 | PF00018 | 0.536 |
LIG_SH3_3 | 120 | 126 | PF00018 | 0.642 |
LIG_SH3_3 | 144 | 150 | PF00018 | 0.678 |
LIG_SH3_3 | 90 | 96 | PF00018 | 0.612 |
LIG_SH3_CIN85_PxpxPR_1 | 92 | 97 | PF14604 | 0.572 |
LIG_SUMO_SIM_par_1 | 366 | 374 | PF11976 | 0.636 |
LIG_TRAF2_1 | 170 | 173 | PF00917 | 0.524 |
LIG_TRAF2_1 | 274 | 277 | PF00917 | 0.523 |
LIG_WW_1 | 14 | 17 | PF00397 | 0.538 |
MOD_CDK_SPK_2 | 92 | 97 | PF00069 | 0.660 |
MOD_CK1_1 | 27 | 33 | PF00069 | 0.685 |
MOD_CK1_1 | 361 | 367 | PF00069 | 0.691 |
MOD_CK1_1 | 380 | 386 | PF00069 | 0.689 |
MOD_CK1_1 | 43 | 49 | PF00069 | 0.439 |
MOD_CK2_1 | 360 | 366 | PF00069 | 0.624 |
MOD_Cter_Amidation | 335 | 338 | PF01082 | 0.659 |
MOD_DYRK1A_RPxSP_1 | 10 | 14 | PF00069 | 0.539 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.705 |
MOD_GlcNHglycan | 338 | 341 | PF01048 | 0.715 |
MOD_GlcNHglycan | 359 | 363 | PF01048 | 0.622 |
MOD_GlcNHglycan | 371 | 376 | PF01048 | 0.701 |
MOD_GlcNHglycan | 382 | 385 | PF01048 | 0.740 |
MOD_GlcNHglycan | 6 | 9 | PF01048 | 0.660 |
MOD_GlcNHglycan | 67 | 70 | PF01048 | 0.675 |
MOD_GlcNHglycan | 98 | 101 | PF01048 | 0.660 |
MOD_GSK3_1 | 108 | 115 | PF00069 | 0.468 |
MOD_GSK3_1 | 332 | 339 | PF00069 | 0.669 |
MOD_GSK3_1 | 371 | 378 | PF00069 | 0.721 |
MOD_GSK3_1 | 380 | 387 | PF00069 | 0.685 |
MOD_GSK3_1 | 4 | 11 | PF00069 | 0.680 |
MOD_GSK3_1 | 408 | 415 | PF00069 | 0.549 |
MOD_GSK3_1 | 67 | 74 | PF00069 | 0.555 |
MOD_GSK3_1 | 92 | 99 | PF00069 | 0.639 |
MOD_N-GLC_1 | 416 | 421 | PF02516 | 0.630 |
MOD_NEK2_1 | 183 | 188 | PF00069 | 0.379 |
MOD_NEK2_1 | 195 | 200 | PF00069 | 0.424 |
MOD_NEK2_1 | 377 | 382 | PF00069 | 0.615 |
MOD_NEK2_1 | 9 | 14 | PF00069 | 0.540 |
MOD_NEK2_2 | 67 | 72 | PF00069 | 0.587 |
MOD_PIKK_1 | 108 | 114 | PF00454 | 0.605 |
MOD_PIKK_1 | 246 | 252 | PF00454 | 0.507 |
MOD_PIKK_1 | 309 | 315 | PF00454 | 0.505 |
MOD_PKA_2 | 140 | 146 | PF00069 | 0.546 |
MOD_PKA_2 | 336 | 342 | PF00069 | 0.674 |
MOD_PKA_2 | 419 | 425 | PF00069 | 0.725 |
MOD_PKA_2 | 65 | 71 | PF00069 | 0.648 |
MOD_PKA_2 | 76 | 82 | PF00069 | 0.626 |
MOD_PKA_2 | 9 | 15 | PF00069 | 0.539 |
MOD_PKA_2 | 96 | 102 | PF00069 | 0.716 |
MOD_Plk_1 | 172 | 178 | PF00069 | 0.441 |
MOD_Plk_1 | 348 | 354 | PF00069 | 0.643 |
MOD_Plk_1 | 75 | 81 | PF00069 | 0.642 |
MOD_Plk_2-3 | 260 | 266 | PF00069 | 0.457 |
MOD_Plk_2-3 | 366 | 372 | PF00069 | 0.676 |
MOD_Plk_4 | 102 | 108 | PF00069 | 0.577 |
MOD_Plk_4 | 128 | 134 | PF00069 | 0.669 |
MOD_Plk_4 | 24 | 30 | PF00069 | 0.606 |
MOD_Plk_4 | 348 | 354 | PF00069 | 0.531 |
MOD_Plk_4 | 419 | 425 | PF00069 | 0.661 |
MOD_ProDKin_1 | 10 | 16 | PF00069 | 0.539 |
MOD_ProDKin_1 | 92 | 98 | PF00069 | 0.680 |
MOD_SUMO_rev_2 | 290 | 300 | PF00179 | 0.414 |
TRG_DiLeu_BaEn_4 | 192 | 198 | PF01217 | 0.540 |
TRG_ENDOCYTIC_2 | 149 | 152 | PF00928 | 0.651 |
TRG_ENDOCYTIC_2 | 28 | 31 | PF00928 | 0.727 |
TRG_ENDOCYTIC_2 | 292 | 295 | PF00928 | 0.532 |
TRG_ENDOCYTIC_2 | 6 | 9 | PF00928 | 0.730 |
TRG_ER_diArg_1 | 18 | 20 | PF00400 | 0.613 |
TRG_ER_diArg_1 | 268 | 270 | PF00400 | 0.458 |
TRG_ER_diArg_1 | 280 | 283 | PF00400 | 0.368 |
TRG_ER_FFAT_2 | 376 | 387 | PF00635 | 0.618 |
TRG_NLS_MonoCore_2 | 424 | 429 | PF00514 | 0.761 |
TRG_NLS_MonoExtC_3 | 424 | 430 | PF00514 | 0.741 |
TRG_Pf-PMV_PEXEL_1 | 308 | 313 | PF00026 | 0.436 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HUH8 | Leptomonas seymouri | 64% | 100% |
A0A1X0NJ59 | Trypanosomatidae | 38% | 100% |
A0A3S7X4V3 | Leishmania donovani | 100% | 100% |
A0A422NPB6 | Trypanosoma rangeli | 39% | 100% |
A4HJR3 | Leishmania braziliensis | 85% | 99% |
C9ZMG1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
E9B274 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
Q4Q5Y5 | Leishmania major | 95% | 100% |
V5D822 | Trypanosoma cruzi | 42% | 100% |