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:0005737 | cytoplasm | 2 | 10 |
GO:0005856 | cytoskeleton | 5 | 9 |
GO:0043226 | organelle | 2 | 9 |
GO:0043228 | non-membrane-bounded organelle | 3 | 9 |
GO:0043229 | intracellular organelle | 3 | 9 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 9 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
GO:0005815 | microtubule organizing center | 2 | 1 |
GO:0005930 | axoneme | 2 | 1 |
GO:0036064 | ciliary basal body | 3 | 1 |
Related structures:
AlphaFold database: A0A3Q8IIC4
Term | Name | Level | Count |
---|---|---|---|
GO:0006996 | organelle organization | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0022607 | cellular component assembly | 4 | 1 |
GO:0030030 | cell projection organization | 4 | 1 |
GO:0030031 | cell projection assembly | 5 | 1 |
GO:0044782 | cilium organization | 5 | 1 |
GO:0060271 | cilium assembly | 6 | 1 |
GO:0070925 | organelle assembly | 5 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:0120031 | plasma membrane bounded cell projection assembly | 6 | 1 |
GO:0120036 | plasma membrane bounded cell projection organization | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 103 | 105 | PF00675 | 0.676 |
CLV_NRD_NRD_1 | 13 | 15 | PF00675 | 0.552 |
CLV_NRD_NRD_1 | 175 | 177 | PF00675 | 0.571 |
CLV_NRD_NRD_1 | 182 | 184 | PF00675 | 0.530 |
CLV_NRD_NRD_1 | 236 | 238 | PF00675 | 0.546 |
CLV_NRD_NRD_1 | 252 | 254 | PF00675 | 0.629 |
CLV_NRD_NRD_1 | 268 | 270 | PF00675 | 0.727 |
CLV_NRD_NRD_1 | 298 | 300 | PF00675 | 0.469 |
CLV_NRD_NRD_1 | 331 | 333 | PF00675 | 0.282 |
CLV_NRD_NRD_1 | 463 | 465 | PF00675 | 0.246 |
CLV_NRD_NRD_1 | 481 | 483 | PF00675 | 0.449 |
CLV_NRD_NRD_1 | 532 | 534 | PF00675 | 0.591 |
CLV_PCSK_FUR_1 | 329 | 333 | PF00082 | 0.331 |
CLV_PCSK_FUR_1 | 394 | 398 | PF00082 | 0.317 |
CLV_PCSK_KEX2_1 | 103 | 105 | PF00082 | 0.676 |
CLV_PCSK_KEX2_1 | 13 | 15 | PF00082 | 0.679 |
CLV_PCSK_KEX2_1 | 175 | 177 | PF00082 | 0.570 |
CLV_PCSK_KEX2_1 | 181 | 183 | PF00082 | 0.536 |
CLV_PCSK_KEX2_1 | 235 | 237 | PF00082 | 0.518 |
CLV_PCSK_KEX2_1 | 268 | 270 | PF00082 | 0.742 |
CLV_PCSK_KEX2_1 | 298 | 300 | PF00082 | 0.409 |
CLV_PCSK_KEX2_1 | 331 | 333 | PF00082 | 0.292 |
CLV_PCSK_KEX2_1 | 396 | 398 | PF00082 | 0.292 |
CLV_PCSK_KEX2_1 | 481 | 483 | PF00082 | 0.519 |
CLV_PCSK_KEX2_1 | 497 | 499 | PF00082 | 0.439 |
CLV_PCSK_PC1ET2_1 | 396 | 398 | PF00082 | 0.317 |
CLV_PCSK_PC1ET2_1 | 497 | 499 | PF00082 | 0.534 |
CLV_PCSK_PC7_1 | 178 | 184 | PF00082 | 0.659 |
CLV_PCSK_PC7_1 | 294 | 300 | PF00082 | 0.415 |
CLV_PCSK_PC7_1 | 477 | 483 | PF00082 | 0.540 |
CLV_PCSK_SKI1_1 | 197 | 201 | PF00082 | 0.509 |
CLV_PCSK_SKI1_1 | 214 | 218 | PF00082 | 0.519 |
CLV_PCSK_SKI1_1 | 249 | 253 | PF00082 | 0.441 |
CLV_PCSK_SKI1_1 | 273 | 277 | PF00082 | 0.587 |
CLV_PCSK_SKI1_1 | 397 | 401 | PF00082 | 0.292 |
CLV_PCSK_SKI1_1 | 457 | 461 | PF00082 | 0.331 |
CLV_PCSK_SKI1_1 | 526 | 530 | PF00082 | 0.552 |
CLV_Separin_Metazoa | 250 | 254 | PF03568 | 0.452 |
CLV_Separin_Metazoa | 291 | 295 | PF03568 | 0.535 |
DEG_APCC_DBOX_1 | 181 | 189 | PF00400 | 0.563 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.700 |
DOC_MAPK_gen_1 | 178 | 188 | PF00069 | 0.470 |
DOC_MAPK_gen_1 | 235 | 242 | PF00069 | 0.449 |
DOC_MAPK_MEF2A_6 | 235 | 244 | PF00069 | 0.468 |
DOC_MAPK_NFAT4_5 | 237 | 245 | PF00069 | 0.429 |
DOC_USP7_MATH_1 | 127 | 131 | PF00917 | 0.592 |
DOC_USP7_MATH_1 | 15 | 19 | PF00917 | 0.739 |
DOC_USP7_MATH_1 | 156 | 160 | PF00917 | 0.570 |
DOC_USP7_MATH_1 | 262 | 266 | PF00917 | 0.576 |
DOC_USP7_MATH_1 | 302 | 306 | PF00917 | 0.592 |
DOC_USP7_MATH_1 | 514 | 518 | PF00917 | 0.664 |
DOC_USP7_MATH_1 | 521 | 525 | PF00917 | 0.658 |
DOC_USP7_MATH_1 | 546 | 550 | PF00917 | 0.615 |
DOC_USP7_MATH_1 | 572 | 576 | PF00917 | 0.700 |
DOC_USP7_UBL2_3 | 396 | 400 | PF12436 | 0.531 |
DOC_WW_Pin1_4 | 133 | 138 | PF00397 | 0.697 |
DOC_WW_Pin1_4 | 152 | 157 | PF00397 | 0.750 |
DOC_WW_Pin1_4 | 267 | 272 | PF00397 | 0.693 |
DOC_WW_Pin1_4 | 539 | 544 | PF00397 | 0.541 |
LIG_14-3-3_CanoR_1 | 175 | 181 | PF00244 | 0.626 |
LIG_14-3-3_CanoR_1 | 182 | 186 | PF00244 | 0.545 |
LIG_14-3-3_CanoR_1 | 298 | 307 | PF00244 | 0.351 |
LIG_14-3-3_CanoR_1 | 487 | 493 | PF00244 | 0.557 |
LIG_Actin_WH2_2 | 238 | 255 | PF00022 | 0.438 |
LIG_CaM_IQ_9 | 418 | 433 | PF13499 | 0.451 |
LIG_Clathr_ClatBox_1 | 185 | 189 | PF01394 | 0.406 |
LIG_FHA_1 | 108 | 114 | PF00498 | 0.445 |
LIG_FHA_1 | 139 | 145 | PF00498 | 0.635 |
LIG_FHA_1 | 203 | 209 | PF00498 | 0.524 |
LIG_FHA_1 | 370 | 376 | PF00498 | 0.480 |
LIG_FHA_1 | 88 | 94 | PF00498 | 0.500 |
LIG_FHA_2 | 208 | 214 | PF00498 | 0.602 |
LIG_FHA_2 | 227 | 233 | PF00498 | 0.400 |
LIG_FHA_2 | 285 | 291 | PF00498 | 0.583 |
LIG_LIR_Gen_1 | 189 | 199 | PF02991 | 0.436 |
LIG_LIR_Gen_1 | 336 | 346 | PF02991 | 0.465 |
LIG_LIR_Gen_1 | 40 | 50 | PF02991 | 0.535 |
LIG_LIR_Nem_3 | 189 | 194 | PF02991 | 0.468 |
LIG_LIR_Nem_3 | 336 | 341 | PF02991 | 0.465 |
LIG_LIR_Nem_3 | 40 | 45 | PF02991 | 0.555 |
LIG_LIR_Nem_3 | 48 | 53 | PF02991 | 0.483 |
LIG_PCNA_yPIPBox_3 | 43 | 52 | PF02747 | 0.563 |
LIG_SH2_CRK | 50 | 54 | PF00017 | 0.443 |
LIG_SH2_GRB2like | 493 | 496 | PF00017 | 0.688 |
LIG_SH2_NCK_1 | 50 | 54 | PF00017 | 0.465 |
LIG_SH2_STAP1 | 50 | 54 | PF00017 | 0.522 |
LIG_SH2_STAT3 | 445 | 448 | PF00017 | 0.436 |
LIG_SH2_STAT5 | 295 | 298 | PF00017 | 0.527 |
LIG_SH2_STAT5 | 306 | 309 | PF00017 | 0.386 |
LIG_SH2_STAT5 | 405 | 408 | PF00017 | 0.436 |
LIG_SH2_STAT5 | 50 | 53 | PF00017 | 0.422 |
LIG_SH3_3 | 108 | 114 | PF00018 | 0.654 |
LIG_SH3_3 | 434 | 440 | PF00018 | 0.449 |
LIG_SH3_3 | 540 | 546 | PF00018 | 0.619 |
LIG_SUMO_SIM_par_1 | 184 | 189 | PF11976 | 0.706 |
LIG_TRAF2_1 | 210 | 213 | PF00917 | 0.561 |
LIG_TRAF2_1 | 229 | 232 | PF00917 | 0.458 |
LIG_TRAF2_1 | 432 | 435 | PF00917 | 0.531 |
LIG_TRAF2_1 | 85 | 88 | PF00917 | 0.593 |
LIG_WRC_WIRS_1 | 46 | 51 | PF05994 | 0.533 |
MOD_CDC14_SPxK_1 | 270 | 273 | PF00782 | 0.529 |
MOD_CDK_SPK_2 | 152 | 157 | PF00069 | 0.514 |
MOD_CDK_SPxK_1 | 267 | 273 | PF00069 | 0.535 |
MOD_CK1_1 | 152 | 158 | PF00069 | 0.622 |
MOD_CK1_1 | 27 | 33 | PF00069 | 0.593 |
MOD_CK1_1 | 371 | 377 | PF00069 | 0.436 |
MOD_CK1_1 | 48 | 54 | PF00069 | 0.543 |
MOD_CK1_1 | 500 | 506 | PF00069 | 0.624 |
MOD_CK1_1 | 524 | 530 | PF00069 | 0.712 |
MOD_CK1_1 | 6 | 12 | PF00069 | 0.627 |
MOD_CK2_1 | 207 | 213 | PF00069 | 0.558 |
MOD_CK2_1 | 226 | 232 | PF00069 | 0.419 |
MOD_CK2_1 | 285 | 291 | PF00069 | 0.601 |
MOD_CK2_1 | 398 | 404 | PF00069 | 0.467 |
MOD_CK2_1 | 541 | 547 | PF00069 | 0.729 |
MOD_Cter_Amidation | 173 | 176 | PF01082 | 0.633 |
MOD_GlcNHglycan | 118 | 121 | PF01048 | 0.683 |
MOD_GlcNHglycan | 128 | 132 | PF01048 | 0.600 |
MOD_GlcNHglycan | 15 | 18 | PF01048 | 0.666 |
MOD_GlcNHglycan | 158 | 161 | PF01048 | 0.626 |
MOD_GlcNHglycan | 168 | 171 | PF01048 | 0.610 |
MOD_GlcNHglycan | 263 | 267 | PF01048 | 0.606 |
MOD_GlcNHglycan | 281 | 284 | PF01048 | 0.624 |
MOD_GlcNHglycan | 30 | 33 | PF01048 | 0.512 |
MOD_GlcNHglycan | 300 | 303 | PF01048 | 0.329 |
MOD_GlcNHglycan | 488 | 491 | PF01048 | 0.479 |
MOD_GlcNHglycan | 502 | 505 | PF01048 | 0.587 |
MOD_GlcNHglycan | 510 | 513 | PF01048 | 0.711 |
MOD_GlcNHglycan | 523 | 526 | PF01048 | 0.646 |
MOD_GlcNHglycan | 55 | 58 | PF01048 | 0.509 |
MOD_GlcNHglycan | 554 | 558 | PF01048 | 0.653 |
MOD_GlcNHglycan | 82 | 86 | PF01048 | 0.487 |
MOD_GSK3_1 | 129 | 136 | PF00069 | 0.657 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.689 |
MOD_GSK3_1 | 166 | 173 | PF00069 | 0.536 |
MOD_GSK3_1 | 23 | 30 | PF00069 | 0.564 |
MOD_GSK3_1 | 298 | 305 | PF00069 | 0.493 |
MOD_GSK3_1 | 367 | 374 | PF00069 | 0.465 |
MOD_GSK3_1 | 400 | 407 | PF00069 | 0.512 |
MOD_GSK3_1 | 41 | 48 | PF00069 | 0.323 |
MOD_GSK3_1 | 5 | 12 | PF00069 | 0.769 |
MOD_GSK3_1 | 502 | 509 | PF00069 | 0.555 |
MOD_GSK3_1 | 70 | 77 | PF00069 | 0.548 |
MOD_N-GLC_1 | 114 | 119 | PF02516 | 0.663 |
MOD_N-GLC_1 | 27 | 32 | PF02516 | 0.584 |
MOD_NEK2_1 | 278 | 283 | PF00069 | 0.631 |
MOD_NEK2_1 | 367 | 372 | PF00069 | 0.436 |
MOD_NEK2_1 | 45 | 50 | PF00069 | 0.535 |
MOD_PIKK_1 | 207 | 213 | PF00454 | 0.523 |
MOD_PKA_1 | 13 | 19 | PF00069 | 0.548 |
MOD_PKA_1 | 181 | 187 | PF00069 | 0.660 |
MOD_PKA_1 | 276 | 282 | PF00069 | 0.549 |
MOD_PKA_1 | 298 | 304 | PF00069 | 0.520 |
MOD_PKA_1 | 497 | 503 | PF00069 | 0.626 |
MOD_PKA_2 | 13 | 19 | PF00069 | 0.578 |
MOD_PKA_2 | 156 | 162 | PF00069 | 0.608 |
MOD_PKA_2 | 181 | 187 | PF00069 | 0.575 |
MOD_PKA_2 | 298 | 304 | PF00069 | 0.520 |
MOD_PKA_2 | 486 | 492 | PF00069 | 0.521 |
MOD_PKA_2 | 497 | 503 | PF00069 | 0.545 |
MOD_PKA_2 | 506 | 512 | PF00069 | 0.583 |
MOD_Plk_1 | 138 | 144 | PF00069 | 0.648 |
MOD_Plk_1 | 546 | 552 | PF00069 | 0.612 |
MOD_Plk_1 | 81 | 87 | PF00069 | 0.581 |
MOD_Plk_2-3 | 547 | 553 | PF00069 | 0.613 |
MOD_Plk_4 | 138 | 144 | PF00069 | 0.676 |
MOD_Plk_4 | 302 | 308 | PF00069 | 0.497 |
MOD_Plk_4 | 41 | 47 | PF00069 | 0.666 |
MOD_ProDKin_1 | 133 | 139 | PF00069 | 0.697 |
MOD_ProDKin_1 | 152 | 158 | PF00069 | 0.752 |
MOD_ProDKin_1 | 267 | 273 | PF00069 | 0.691 |
MOD_ProDKin_1 | 539 | 545 | PF00069 | 0.542 |
MOD_SUMO_for_1 | 395 | 398 | PF00179 | 0.517 |
MOD_SUMO_for_1 | 440 | 443 | PF00179 | 0.446 |
MOD_SUMO_rev_2 | 189 | 199 | PF00179 | 0.525 |
MOD_SUMO_rev_2 | 258 | 262 | PF00179 | 0.525 |
MOD_SUMO_rev_2 | 270 | 278 | PF00179 | 0.473 |
MOD_SUMO_rev_2 | 344 | 353 | PF00179 | 0.471 |
MOD_SUMO_rev_2 | 363 | 370 | PF00179 | 0.362 |
MOD_SUMO_rev_2 | 419 | 428 | PF00179 | 0.453 |
TRG_DiLeu_BaEn_4 | 88 | 94 | PF01217 | 0.476 |
TRG_ENDOCYTIC_2 | 50 | 53 | PF00928 | 0.442 |
TRG_ER_diArg_1 | 103 | 105 | PF00400 | 0.608 |
TRG_ER_diArg_1 | 175 | 178 | PF00400 | 0.586 |
TRG_ER_diArg_1 | 180 | 183 | PF00400 | 0.568 |
TRG_ER_diArg_1 | 234 | 237 | PF00400 | 0.513 |
TRG_ER_diArg_1 | 328 | 331 | PF00400 | 0.449 |
TRG_ER_diArg_1 | 481 | 483 | PF00400 | 0.525 |
TRG_Pf-PMV_PEXEL_1 | 183 | 187 | PF00026 | 0.591 |
TRG_Pf-PMV_PEXEL_1 | 362 | 366 | PF00026 | 0.251 |
TRG_Pf-PMV_PEXEL_1 | 481 | 486 | PF00026 | 0.642 |
TRG_Pf-PMV_PEXEL_1 | 526 | 531 | PF00026 | 0.719 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5T9 | Leptomonas seymouri | 63% | 100% |
A0A1X0NNL2 | Trypanosomatidae | 40% | 100% |
A0A422N1M9 | Trypanosoma rangeli | 39% | 100% |
A4H7N6 | Leishmania braziliensis | 78% | 100% |
A4HW26 | Leishmania infantum | 99% | 100% |
C9ZT07 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 100% |
E9APS7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
Q4QFQ1 | Leishmania major | 93% | 100% |
V5BEA4 | Trypanosoma cruzi | 42% | 100% |