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:0005929 | cilium | 4 | 1 |
GO:0042995 | cell projection | 2 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 1 |
Related structures:
AlphaFold database: E9B2F6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 100 | 102 | PF00675 | 0.514 |
CLV_NRD_NRD_1 | 126 | 128 | PF00675 | 0.508 |
CLV_NRD_NRD_1 | 437 | 439 | PF00675 | 0.374 |
CLV_NRD_NRD_1 | 83 | 85 | PF00675 | 0.634 |
CLV_PCSK_KEX2_1 | 126 | 128 | PF00082 | 0.508 |
CLV_PCSK_KEX2_1 | 437 | 439 | PF00082 | 0.612 |
CLV_PCSK_KEX2_1 | 451 | 453 | PF00082 | 0.458 |
CLV_PCSK_KEX2_1 | 82 | 84 | PF00082 | 0.636 |
CLV_PCSK_KEX2_1 | 99 | 101 | PF00082 | 0.527 |
CLV_PCSK_PC1ET2_1 | 451 | 453 | PF00082 | 0.592 |
CLV_PCSK_PC1ET2_1 | 82 | 84 | PF00082 | 0.626 |
CLV_PCSK_SKI1_1 | 126 | 130 | PF00082 | 0.633 |
CLV_PCSK_SKI1_1 | 460 | 464 | PF00082 | 0.609 |
CLV_PCSK_SKI1_1 | 59 | 63 | PF00082 | 0.548 |
CLV_PCSK_SKI1_1 | 84 | 88 | PF00082 | 0.490 |
DEG_APCC_DBOX_1 | 100 | 108 | PF00400 | 0.498 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.470 |
DOC_MAPK_gen_1 | 123 | 131 | PF00069 | 0.537 |
DOC_MAPK_gen_1 | 379 | 389 | PF00069 | 0.729 |
DOC_MAPK_gen_1 | 82 | 91 | PF00069 | 0.613 |
DOC_MAPK_gen_1 | 99 | 110 | PF00069 | 0.513 |
DOC_PP2B_LxvP_1 | 129 | 132 | PF13499 | 0.571 |
DOC_USP7_MATH_1 | 141 | 145 | PF00917 | 0.752 |
DOC_USP7_MATH_1 | 194 | 198 | PF00917 | 0.676 |
DOC_USP7_MATH_1 | 251 | 255 | PF00917 | 0.668 |
DOC_USP7_MATH_1 | 26 | 30 | PF00917 | 0.624 |
DOC_USP7_MATH_1 | 292 | 296 | PF00917 | 0.724 |
DOC_USP7_MATH_1 | 317 | 321 | PF00917 | 0.649 |
DOC_USP7_MATH_1 | 458 | 462 | PF00917 | 0.695 |
DOC_USP7_UBL2_3 | 447 | 451 | PF12436 | 0.593 |
DOC_USP7_UBL2_3 | 66 | 70 | PF12436 | 0.558 |
DOC_WW_Pin1_4 | 165 | 170 | PF00397 | 0.732 |
DOC_WW_Pin1_4 | 247 | 252 | PF00397 | 0.643 |
LIG_14-3-3_CanoR_1 | 11 | 15 | PF00244 | 0.555 |
LIG_14-3-3_CanoR_1 | 161 | 169 | PF00244 | 0.731 |
LIG_14-3-3_CanoR_1 | 172 | 179 | PF00244 | 0.639 |
LIG_14-3-3_CanoR_1 | 300 | 305 | PF00244 | 0.634 |
LIG_14-3-3_CanoR_1 | 335 | 341 | PF00244 | 0.725 |
LIG_Actin_WH2_2 | 309 | 324 | PF00022 | 0.453 |
LIG_BRCT_BRCA1_1 | 253 | 257 | PF00533 | 0.631 |
LIG_BRCT_BRCA1_1 | 280 | 284 | PF00533 | 0.614 |
LIG_BRCT_BRCA1_1 | 332 | 336 | PF00533 | 0.721 |
LIG_Clathr_ClatBox_1 | 107 | 111 | PF01394 | 0.467 |
LIG_eIF4E_1 | 207 | 213 | PF01652 | 0.512 |
LIG_FHA_1 | 258 | 264 | PF00498 | 0.664 |
LIG_FHA_1 | 309 | 315 | PF00498 | 0.672 |
LIG_FHA_1 | 358 | 364 | PF00498 | 0.666 |
LIG_FHA_1 | 384 | 390 | PF00498 | 0.731 |
LIG_FHA_2 | 426 | 432 | PF00498 | 0.552 |
LIG_LIR_Gen_1 | 29 | 37 | PF02991 | 0.515 |
LIG_LIR_Nem_3 | 359 | 364 | PF02991 | 0.583 |
LIG_PAM2_1 | 22 | 34 | PF00658 | 0.531 |
LIG_Pex14_2 | 336 | 340 | PF04695 | 0.726 |
LIG_SH2_STAP1 | 454 | 458 | PF00017 | 0.528 |
LIG_SH2_STAT3 | 14 | 17 | PF00017 | 0.582 |
LIG_SH2_STAT5 | 14 | 17 | PF00017 | 0.476 |
LIG_SH2_STAT5 | 9 | 12 | PF00017 | 0.479 |
LIG_SH3_3 | 260 | 266 | PF00018 | 0.639 |
LIG_SH3_3 | 274 | 280 | PF00018 | 0.714 |
LIG_SH3_3 | 311 | 317 | PF00018 | 0.590 |
LIG_SH3_3 | 37 | 43 | PF00018 | 0.349 |
LIG_SH3_3 | 410 | 416 | PF00018 | 0.719 |
LIG_SUMO_SIM_anti_2 | 106 | 111 | PF11976 | 0.470 |
LIG_SUMO_SIM_par_1 | 106 | 111 | PF11976 | 0.470 |
LIG_TRAF2_1 | 132 | 135 | PF00917 | 0.601 |
LIG_TRAF2_1 | 349 | 352 | PF00917 | 0.676 |
MOD_CDK_SPxxK_3 | 165 | 172 | PF00069 | 0.710 |
MOD_CK1_1 | 146 | 152 | PF00069 | 0.764 |
MOD_CK1_1 | 154 | 160 | PF00069 | 0.728 |
MOD_CK1_1 | 171 | 177 | PF00069 | 0.659 |
MOD_CK1_1 | 299 | 305 | PF00069 | 0.749 |
MOD_CK1_1 | 346 | 352 | PF00069 | 0.664 |
MOD_CK1_1 | 394 | 400 | PF00069 | 0.682 |
MOD_CK2_1 | 150 | 156 | PF00069 | 0.746 |
MOD_CK2_1 | 346 | 352 | PF00069 | 0.640 |
MOD_CK2_1 | 390 | 396 | PF00069 | 0.796 |
MOD_Cter_Amidation | 295 | 298 | PF01082 | 0.609 |
MOD_GlcNHglycan | 139 | 142 | PF01048 | 0.730 |
MOD_GlcNHglycan | 145 | 148 | PF01048 | 0.738 |
MOD_GlcNHglycan | 163 | 166 | PF01048 | 0.635 |
MOD_GlcNHglycan | 173 | 176 | PF01048 | 0.480 |
MOD_GlcNHglycan | 247 | 250 | PF01048 | 0.722 |
MOD_GlcNHglycan | 279 | 283 | PF01048 | 0.699 |
MOD_GlcNHglycan | 294 | 297 | PF01048 | 0.670 |
MOD_GlcNHglycan | 326 | 329 | PF01048 | 0.754 |
MOD_GlcNHglycan | 345 | 348 | PF01048 | 0.756 |
MOD_GlcNHglycan | 420 | 423 | PF01048 | 0.587 |
MOD_GlcNHglycan | 460 | 463 | PF01048 | 0.577 |
MOD_GSK3_1 | 137 | 144 | PF00069 | 0.772 |
MOD_GSK3_1 | 146 | 153 | PF00069 | 0.704 |
MOD_GSK3_1 | 161 | 168 | PF00069 | 0.732 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.602 |
MOD_GSK3_1 | 247 | 254 | PF00069 | 0.630 |
MOD_GSK3_1 | 26 | 33 | PF00069 | 0.509 |
MOD_GSK3_1 | 292 | 299 | PF00069 | 0.662 |
MOD_GSK3_1 | 390 | 397 | PF00069 | 0.730 |
MOD_GSK3_1 | 414 | 421 | PF00069 | 0.621 |
MOD_GSK3_1 | 454 | 461 | PF00069 | 0.620 |
MOD_GSK3_1 | 48 | 55 | PF00069 | 0.476 |
MOD_N-GLC_1 | 284 | 289 | PF02516 | 0.729 |
MOD_N-GLC_1 | 394 | 399 | PF02516 | 0.697 |
MOD_N-GLC_1 | 418 | 423 | PF02516 | 0.729 |
MOD_NEK2_1 | 212 | 217 | PF00069 | 0.646 |
MOD_NEK2_1 | 257 | 262 | PF00069 | 0.516 |
MOD_NEK2_1 | 284 | 289 | PF00069 | 0.674 |
MOD_NEK2_1 | 336 | 341 | PF00069 | 0.656 |
MOD_NEK2_1 | 424 | 429 | PF00069 | 0.543 |
MOD_NEK2_1 | 52 | 57 | PF00069 | 0.481 |
MOD_NEK2_1 | 61 | 66 | PF00069 | 0.476 |
MOD_NEK2_1 | 77 | 82 | PF00069 | 0.535 |
MOD_NEK2_2 | 317 | 322 | PF00069 | 0.456 |
MOD_NEK2_2 | 383 | 388 | PF00069 | 0.663 |
MOD_NEK2_2 | 48 | 53 | PF00069 | 0.549 |
MOD_PIKK_1 | 212 | 218 | PF00454 | 0.592 |
MOD_PIKK_1 | 322 | 328 | PF00454 | 0.591 |
MOD_PIKK_1 | 395 | 401 | PF00454 | 0.725 |
MOD_PKA_1 | 217 | 223 | PF00069 | 0.570 |
MOD_PKA_2 | 10 | 16 | PF00069 | 0.561 |
MOD_PKA_2 | 150 | 156 | PF00069 | 0.775 |
MOD_PKA_2 | 160 | 166 | PF00069 | 0.727 |
MOD_PKA_2 | 171 | 177 | PF00069 | 0.651 |
MOD_PKA_2 | 299 | 305 | PF00069 | 0.702 |
MOD_PKA_2 | 336 | 342 | PF00069 | 0.711 |
MOD_Plk_1 | 20 | 26 | PF00069 | 0.679 |
MOD_Plk_1 | 284 | 290 | PF00069 | 0.599 |
MOD_Plk_4 | 178 | 184 | PF00069 | 0.419 |
MOD_Plk_4 | 26 | 32 | PF00069 | 0.579 |
MOD_ProDKin_1 | 165 | 171 | PF00069 | 0.728 |
MOD_ProDKin_1 | 247 | 253 | PF00069 | 0.643 |
MOD_SUMO_rev_2 | 398 | 408 | PF00179 | 0.717 |
MOD_SUMO_rev_2 | 79 | 89 | PF00179 | 0.619 |
TRG_ER_diArg_1 | 436 | 438 | PF00400 | 0.379 |
TRG_ER_diArg_1 | 98 | 101 | PF00400 | 0.523 |
TRG_NLS_MonoExtC_3 | 216 | 221 | PF00514 | 0.605 |
TRG_Pf-PMV_PEXEL_1 | 187 | 191 | PF00026 | 0.589 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PE29 | Leptomonas seymouri | 66% | 98% |
A0A1X0P7K1 | Trypanosomatidae | 37% | 100% |
A0A3Q8ICW8 | Leishmania donovani | 95% | 100% |
A0A3R7NTG2 | Trypanosoma rangeli | 36% | 100% |
A4HK15 | Leishmania braziliensis | 83% | 100% |
A4I7J9 | Leishmania infantum | 95% | 100% |
D0A0A1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
Q4Q5Q0 | Leishmania major | 93% | 100% |
V5BS76 | Trypanosoma cruzi | 35% | 100% |