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: A4HK15
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 222 | 226 | PF00656 | 0.608 |
CLV_C14_Caspase3-7 | 327 | 331 | PF00656 | 0.535 |
CLV_NRD_NRD_1 | 100 | 102 | PF00675 | 0.533 |
CLV_NRD_NRD_1 | 126 | 128 | PF00675 | 0.517 |
CLV_NRD_NRD_1 | 323 | 325 | PF00675 | 0.552 |
CLV_NRD_NRD_1 | 80 | 82 | PF00675 | 0.667 |
CLV_NRD_NRD_1 | 83 | 85 | PF00675 | 0.652 |
CLV_PCSK_FUR_1 | 81 | 85 | PF00082 | 0.435 |
CLV_PCSK_KEX2_1 | 126 | 128 | PF00082 | 0.517 |
CLV_PCSK_KEX2_1 | 323 | 325 | PF00082 | 0.557 |
CLV_PCSK_KEX2_1 | 435 | 437 | PF00082 | 0.612 |
CLV_PCSK_KEX2_1 | 449 | 451 | PF00082 | 0.462 |
CLV_PCSK_KEX2_1 | 82 | 84 | PF00082 | 0.663 |
CLV_PCSK_KEX2_1 | 99 | 101 | PF00082 | 0.544 |
CLV_PCSK_PC1ET2_1 | 435 | 437 | PF00082 | 0.589 |
CLV_PCSK_PC1ET2_1 | 449 | 451 | PF00082 | 0.595 |
CLV_PCSK_PC1ET2_1 | 82 | 84 | PF00082 | 0.655 |
CLV_PCSK_SKI1_1 | 126 | 130 | PF00082 | 0.630 |
CLV_PCSK_SKI1_1 | 184 | 188 | PF00082 | 0.425 |
CLV_PCSK_SKI1_1 | 370 | 374 | PF00082 | 0.697 |
CLV_PCSK_SKI1_1 | 385 | 389 | PF00082 | 0.682 |
CLV_PCSK_SKI1_1 | 59 | 63 | PF00082 | 0.558 |
CLV_PCSK_SKI1_1 | 66 | 70 | PF00082 | 0.575 |
CLV_PCSK_SKI1_1 | 84 | 88 | PF00082 | 0.585 |
DEG_APCC_DBOX_1 | 100 | 108 | PF00400 | 0.499 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.516 |
DOC_MAPK_gen_1 | 123 | 131 | PF00069 | 0.548 |
DOC_MAPK_gen_1 | 379 | 389 | PF00069 | 0.747 |
DOC_MAPK_gen_1 | 81 | 91 | PF00069 | 0.640 |
DOC_MAPK_gen_1 | 99 | 110 | PF00069 | 0.495 |
DOC_PP2B_LxvP_1 | 129 | 132 | PF13499 | 0.574 |
DOC_USP7_MATH_1 | 194 | 198 | PF00917 | 0.677 |
DOC_USP7_MATH_1 | 251 | 255 | PF00917 | 0.634 |
DOC_USP7_MATH_1 | 26 | 30 | PF00917 | 0.692 |
DOC_USP7_MATH_1 | 292 | 296 | PF00917 | 0.678 |
DOC_USP7_MATH_1 | 317 | 321 | PF00917 | 0.677 |
DOC_USP7_MATH_1 | 378 | 382 | PF00917 | 0.664 |
DOC_USP7_MATH_1 | 456 | 460 | PF00917 | 0.699 |
DOC_USP7_MATH_2 | 317 | 323 | PF00917 | 0.516 |
DOC_USP7_UBL2_3 | 445 | 449 | PF12436 | 0.599 |
DOC_USP7_UBL2_3 | 66 | 70 | PF12436 | 0.548 |
DOC_WW_Pin1_4 | 165 | 170 | PF00397 | 0.717 |
LIG_14-3-3_CanoR_1 | 161 | 169 | PF00244 | 0.735 |
LIG_14-3-3_CanoR_1 | 172 | 179 | PF00244 | 0.622 |
LIG_14-3-3_CanoR_1 | 335 | 341 | PF00244 | 0.737 |
LIG_BRCT_BRCA1_1 | 253 | 257 | PF00533 | 0.597 |
LIG_BRCT_BRCA1_1 | 332 | 336 | PF00533 | 0.740 |
LIG_Clathr_ClatBox_1 | 107 | 111 | PF01394 | 0.463 |
LIG_eIF4E_1 | 207 | 213 | PF01652 | 0.522 |
LIG_FHA_1 | 258 | 264 | PF00498 | 0.615 |
LIG_FHA_1 | 309 | 315 | PF00498 | 0.686 |
LIG_FHA_1 | 358 | 364 | PF00498 | 0.640 |
LIG_FHA_1 | 384 | 390 | PF00498 | 0.756 |
LIG_FHA_1 | 458 | 464 | PF00498 | 0.591 |
LIG_FHA_2 | 424 | 430 | PF00498 | 0.551 |
LIG_LIR_Nem_3 | 359 | 364 | PF02991 | 0.554 |
LIG_Pex14_2 | 280 | 284 | PF04695 | 0.423 |
LIG_Pex14_2 | 336 | 340 | PF04695 | 0.737 |
LIG_SH2_STAP1 | 452 | 456 | PF00017 | 0.530 |
LIG_SH2_STAT3 | 14 | 17 | PF00017 | 0.612 |
LIG_SH2_STAT5 | 14 | 17 | PF00017 | 0.477 |
LIG_SH2_STAT5 | 9 | 12 | PF00017 | 0.504 |
LIG_SH3_3 | 136 | 142 | PF00018 | 0.539 |
LIG_SH3_3 | 260 | 266 | PF00018 | 0.593 |
LIG_SH3_3 | 311 | 317 | PF00018 | 0.608 |
LIG_SH3_3 | 408 | 414 | PF00018 | 0.793 |
LIG_SUMO_SIM_anti_2 | 106 | 111 | PF11976 | 0.466 |
LIG_SUMO_SIM_par_1 | 106 | 111 | PF11976 | 0.466 |
LIG_TRAF2_1 | 349 | 352 | PF00917 | 0.685 |
LIG_UBA3_1 | 182 | 187 | PF00899 | 0.475 |
MOD_CDK_SPxxK_3 | 165 | 172 | PF00069 | 0.750 |
MOD_CK1_1 | 13 | 19 | PF00069 | 0.514 |
MOD_CK1_1 | 144 | 150 | PF00069 | 0.770 |
MOD_CK1_1 | 154 | 160 | PF00069 | 0.658 |
MOD_CK1_1 | 171 | 177 | PF00069 | 0.495 |
MOD_CK1_1 | 299 | 305 | PF00069 | 0.748 |
MOD_CK1_1 | 394 | 400 | PF00069 | 0.703 |
MOD_CK1_1 | 457 | 463 | PF00069 | 0.472 |
MOD_CK2_1 | 378 | 384 | PF00069 | 0.714 |
MOD_CK2_1 | 390 | 396 | PF00069 | 0.805 |
MOD_Cter_Amidation | 295 | 298 | PF01082 | 0.577 |
MOD_GlcNHglycan | 136 | 142 | PF01048 | 0.721 |
MOD_GlcNHglycan | 145 | 149 | PF01048 | 0.712 |
MOD_GlcNHglycan | 163 | 166 | PF01048 | 0.655 |
MOD_GlcNHglycan | 173 | 176 | PF01048 | 0.472 |
MOD_GlcNHglycan | 247 | 250 | PF01048 | 0.666 |
MOD_GlcNHglycan | 294 | 297 | PF01048 | 0.599 |
MOD_GlcNHglycan | 418 | 421 | PF01048 | 0.590 |
MOD_GSK3_1 | 137 | 144 | PF00069 | 0.777 |
MOD_GSK3_1 | 147 | 154 | PF00069 | 0.689 |
MOD_GSK3_1 | 161 | 168 | PF00069 | 0.727 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.610 |
MOD_GSK3_1 | 280 | 287 | PF00069 | 0.539 |
MOD_GSK3_1 | 292 | 299 | PF00069 | 0.627 |
MOD_GSK3_1 | 390 | 397 | PF00069 | 0.753 |
MOD_GSK3_1 | 452 | 459 | PF00069 | 0.623 |
MOD_GSK3_1 | 48 | 55 | PF00069 | 0.505 |
MOD_N-GLC_1 | 284 | 289 | PF02516 | 0.660 |
MOD_N-GLC_1 | 330 | 335 | PF02516 | 0.650 |
MOD_N-GLC_1 | 394 | 399 | PF02516 | 0.714 |
MOD_N-GLC_1 | 416 | 421 | PF02516 | 0.530 |
MOD_N-GLC_2 | 235 | 237 | PF02516 | 0.549 |
MOD_NEK2_1 | 212 | 217 | PF00069 | 0.655 |
MOD_NEK2_1 | 257 | 262 | PF00069 | 0.481 |
MOD_NEK2_1 | 280 | 285 | PF00069 | 0.626 |
MOD_NEK2_1 | 336 | 341 | PF00069 | 0.665 |
MOD_NEK2_1 | 415 | 420 | PF00069 | 0.598 |
MOD_NEK2_1 | 422 | 427 | PF00069 | 0.547 |
MOD_NEK2_1 | 52 | 57 | PF00069 | 0.510 |
MOD_NEK2_1 | 61 | 66 | PF00069 | 0.481 |
MOD_NEK2_1 | 77 | 82 | PF00069 | 0.533 |
MOD_NEK2_2 | 26 | 31 | PF00069 | 0.541 |
MOD_NEK2_2 | 48 | 53 | PF00069 | 0.580 |
MOD_PIKK_1 | 13 | 19 | PF00454 | 0.471 |
MOD_PIKK_1 | 212 | 218 | PF00454 | 0.604 |
MOD_PIKK_1 | 317 | 323 | PF00454 | 0.652 |
MOD_PIKK_1 | 371 | 377 | PF00454 | 0.631 |
MOD_PIKK_1 | 395 | 401 | PF00454 | 0.744 |
MOD_PKA_1 | 217 | 223 | PF00069 | 0.597 |
MOD_PKA_2 | 160 | 166 | PF00069 | 0.712 |
MOD_PKA_2 | 171 | 177 | PF00069 | 0.644 |
MOD_PKA_2 | 223 | 229 | PF00069 | 0.480 |
MOD_PKA_2 | 325 | 331 | PF00069 | 0.773 |
MOD_PKA_2 | 336 | 342 | PF00069 | 0.719 |
MOD_PKA_2 | 457 | 463 | PF00069 | 0.601 |
MOD_Plk_1 | 20 | 26 | PF00069 | 0.719 |
MOD_Plk_1 | 383 | 389 | PF00069 | 0.617 |
MOD_ProDKin_1 | 165 | 171 | PF00069 | 0.713 |
MOD_SUMO_rev_2 | 429 | 437 | PF00179 | 0.642 |
MOD_SUMO_rev_2 | 79 | 89 | PF00179 | 0.645 |
TRG_ER_diArg_1 | 323 | 326 | PF00400 | 0.555 |
TRG_ER_diArg_1 | 81 | 84 | PF00400 | 0.442 |
TRG_ER_diArg_1 | 98 | 101 | PF00400 | 0.543 |
TRG_NLS_MonoExtC_3 | 216 | 221 | PF00514 | 0.626 |
TRG_Pf-PMV_PEXEL_1 | 184 | 188 | PF00026 | 0.361 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PE29 | Leptomonas seymouri | 63% | 97% |
A0A1X0P7K1 | Trypanosomatidae | 37% | 100% |
A0A3Q8ICW8 | Leishmania donovani | 83% | 100% |
A0A3R7NTG2 | Trypanosoma rangeli | 35% | 100% |
A4I7J9 | Leishmania infantum | 83% | 100% |
D0A0A1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
E9B2F6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |
Q4Q5Q0 | Leishmania major | 82% | 100% |
V5BS76 | Trypanosoma cruzi | 34% | 100% |