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 | 2 |
GO:0042995 | cell projection | 2 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 2 |
Related structures:
AlphaFold database: Q4Q5Q0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 222 | 226 | PF00656 | 0.542 |
CLV_NRD_NRD_1 | 100 | 102 | PF00675 | 0.361 |
CLV_NRD_NRD_1 | 126 | 128 | PF00675 | 0.476 |
CLV_NRD_NRD_1 | 83 | 85 | PF00675 | 0.609 |
CLV_PCSK_KEX2_1 | 126 | 128 | PF00082 | 0.516 |
CLV_PCSK_KEX2_1 | 440 | 442 | PF00082 | 0.526 |
CLV_PCSK_KEX2_1 | 454 | 456 | PF00082 | 0.420 |
CLV_PCSK_KEX2_1 | 82 | 84 | PF00082 | 0.633 |
CLV_PCSK_KEX2_1 | 99 | 101 | PF00082 | 0.379 |
CLV_PCSK_PC1ET2_1 | 440 | 442 | PF00082 | 0.509 |
CLV_PCSK_PC1ET2_1 | 454 | 456 | PF00082 | 0.555 |
CLV_PCSK_PC1ET2_1 | 82 | 84 | PF00082 | 0.633 |
CLV_PCSK_SKI1_1 | 126 | 130 | PF00082 | 0.627 |
CLV_PCSK_SKI1_1 | 370 | 374 | PF00082 | 0.659 |
CLV_PCSK_SKI1_1 | 385 | 389 | PF00082 | 0.635 |
CLV_PCSK_SKI1_1 | 463 | 467 | PF00082 | 0.518 |
CLV_PCSK_SKI1_1 | 59 | 63 | PF00082 | 0.521 |
CLV_PCSK_SKI1_1 | 84 | 88 | PF00082 | 0.517 |
DEG_APCC_DBOX_1 | 100 | 108 | PF00400 | 0.463 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.450 |
DOC_MAPK_gen_1 | 123 | 131 | PF00069 | 0.508 |
DOC_MAPK_gen_1 | 379 | 389 | PF00069 | 0.652 |
DOC_MAPK_gen_1 | 82 | 91 | PF00069 | 0.609 |
DOC_MAPK_gen_1 | 99 | 110 | PF00069 | 0.383 |
DOC_PP2B_LxvP_1 | 129 | 132 | PF13499 | 0.559 |
DOC_USP7_MATH_1 | 194 | 198 | PF00917 | 0.651 |
DOC_USP7_MATH_1 | 251 | 255 | PF00917 | 0.660 |
DOC_USP7_MATH_1 | 26 | 30 | PF00917 | 0.605 |
DOC_USP7_MATH_1 | 292 | 296 | PF00917 | 0.732 |
DOC_USP7_MATH_1 | 317 | 321 | PF00917 | 0.651 |
DOC_USP7_MATH_1 | 391 | 395 | PF00917 | 0.631 |
DOC_USP7_MATH_1 | 40 | 44 | PF00917 | 0.579 |
DOC_USP7_MATH_1 | 461 | 465 | PF00917 | 0.648 |
DOC_USP7_UBL2_3 | 450 | 454 | PF12436 | 0.564 |
DOC_USP7_UBL2_3 | 66 | 70 | PF12436 | 0.519 |
DOC_WW_Pin1_4 | 143 | 148 | PF00397 | 0.717 |
DOC_WW_Pin1_4 | 165 | 170 | PF00397 | 0.698 |
DOC_WW_Pin1_4 | 247 | 252 | PF00397 | 0.564 |
DOC_WW_Pin1_4 | 370 | 375 | PF00397 | 0.664 |
LIG_14-3-3_CanoR_1 | 11 | 15 | PF00244 | 0.559 |
LIG_14-3-3_CanoR_1 | 161 | 169 | PF00244 | 0.716 |
LIG_14-3-3_CanoR_1 | 172 | 179 | PF00244 | 0.612 |
LIG_14-3-3_CanoR_1 | 300 | 305 | PF00244 | 0.669 |
LIG_14-3-3_CanoR_1 | 335 | 341 | PF00244 | 0.708 |
LIG_BRCT_BRCA1_1 | 253 | 257 | PF00533 | 0.614 |
LIG_BRCT_BRCA1_1 | 280 | 284 | PF00533 | 0.567 |
LIG_BRCT_BRCA1_1 | 332 | 336 | PF00533 | 0.707 |
LIG_Clathr_ClatBox_1 | 107 | 111 | PF01394 | 0.473 |
LIG_eIF4E_1 | 207 | 213 | PF01652 | 0.450 |
LIG_FHA_1 | 258 | 264 | PF00498 | 0.653 |
LIG_FHA_1 | 309 | 315 | PF00498 | 0.641 |
LIG_FHA_1 | 358 | 364 | PF00498 | 0.645 |
LIG_FHA_1 | 384 | 390 | PF00498 | 0.654 |
LIG_FHA_2 | 274 | 280 | PF00498 | 0.557 |
LIG_FHA_2 | 347 | 353 | PF00498 | 0.538 |
LIG_FHA_2 | 429 | 435 | PF00498 | 0.501 |
LIG_LIR_Gen_1 | 29 | 37 | PF02991 | 0.471 |
LIG_LIR_Nem_3 | 359 | 364 | PF02991 | 0.554 |
LIG_PAM2_1 | 22 | 34 | PF00658 | 0.486 |
LIG_PDZ_Class_2 | 465 | 470 | PF00595 | 0.518 |
LIG_Pex14_2 | 336 | 340 | PF04695 | 0.710 |
LIG_SH2_STAP1 | 421 | 425 | PF00017 | 0.537 |
LIG_SH2_STAP1 | 457 | 461 | PF00017 | 0.478 |
LIG_SH2_STAT3 | 14 | 17 | PF00017 | 0.575 |
LIG_SH2_STAT5 | 14 | 17 | PF00017 | 0.416 |
LIG_SH2_STAT5 | 9 | 12 | PF00017 | 0.419 |
LIG_SH3_3 | 260 | 266 | PF00018 | 0.608 |
LIG_SH3_3 | 311 | 317 | PF00018 | 0.581 |
LIG_SH3_3 | 413 | 419 | PF00018 | 0.640 |
LIG_SUMO_SIM_anti_2 | 106 | 111 | PF11976 | 0.431 |
LIG_SUMO_SIM_par_1 | 106 | 111 | PF11976 | 0.469 |
LIG_TRAF2_1 | 132 | 135 | PF00917 | 0.581 |
LIG_TRAF2_1 | 349 | 352 | PF00917 | 0.610 |
MOD_CDK_SPxxK_3 | 165 | 172 | PF00069 | 0.741 |
MOD_CK1_1 | 146 | 152 | PF00069 | 0.711 |
MOD_CK1_1 | 154 | 160 | PF00069 | 0.722 |
MOD_CK1_1 | 171 | 177 | PF00069 | 0.445 |
MOD_CK1_1 | 299 | 305 | PF00069 | 0.753 |
MOD_CK1_1 | 346 | 352 | PF00069 | 0.623 |
MOD_CK1_1 | 394 | 400 | PF00069 | 0.643 |
MOD_CK2_1 | 150 | 156 | PF00069 | 0.697 |
MOD_CK2_1 | 273 | 279 | PF00069 | 0.540 |
MOD_CK2_1 | 346 | 352 | PF00069 | 0.615 |
MOD_CK2_1 | 390 | 396 | PF00069 | 0.769 |
MOD_CK2_1 | 40 | 46 | PF00069 | 0.419 |
MOD_GlcNHglycan | 139 | 142 | PF01048 | 0.746 |
MOD_GlcNHglycan | 163 | 166 | PF01048 | 0.634 |
MOD_GlcNHglycan | 173 | 176 | PF01048 | 0.435 |
MOD_GlcNHglycan | 247 | 250 | PF01048 | 0.628 |
MOD_GlcNHglycan | 279 | 283 | PF01048 | 0.687 |
MOD_GlcNHglycan | 294 | 297 | PF01048 | 0.621 |
MOD_GlcNHglycan | 326 | 329 | PF01048 | 0.755 |
MOD_GlcNHglycan | 345 | 348 | PF01048 | 0.733 |
MOD_GlcNHglycan | 423 | 426 | PF01048 | 0.546 |
MOD_GlcNHglycan | 463 | 466 | PF01048 | 0.514 |
MOD_GSK3_1 | 137 | 144 | PF00069 | 0.777 |
MOD_GSK3_1 | 146 | 153 | PF00069 | 0.676 |
MOD_GSK3_1 | 161 | 168 | PF00069 | 0.714 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.561 |
MOD_GSK3_1 | 247 | 254 | PF00069 | 0.603 |
MOD_GSK3_1 | 292 | 299 | PF00069 | 0.594 |
MOD_GSK3_1 | 390 | 397 | PF00069 | 0.696 |
MOD_GSK3_1 | 417 | 424 | PF00069 | 0.558 |
MOD_GSK3_1 | 457 | 464 | PF00069 | 0.570 |
MOD_GSK3_1 | 48 | 55 | PF00069 | 0.441 |
MOD_N-GLC_1 | 284 | 289 | PF02516 | 0.719 |
MOD_N-GLC_1 | 394 | 399 | PF02516 | 0.659 |
MOD_NEK2_1 | 212 | 217 | PF00069 | 0.503 |
MOD_NEK2_1 | 257 | 262 | PF00069 | 0.510 |
MOD_NEK2_1 | 284 | 289 | PF00069 | 0.676 |
MOD_NEK2_1 | 336 | 341 | PF00069 | 0.620 |
MOD_NEK2_1 | 427 | 432 | PF00069 | 0.505 |
MOD_NEK2_1 | 52 | 57 | PF00069 | 0.460 |
MOD_NEK2_1 | 61 | 66 | PF00069 | 0.485 |
MOD_NEK2_1 | 77 | 82 | PF00069 | 0.508 |
MOD_NEK2_2 | 383 | 388 | PF00069 | 0.603 |
MOD_NEK2_2 | 48 | 53 | PF00069 | 0.484 |
MOD_PIKK_1 | 212 | 218 | PF00454 | 0.561 |
MOD_PIKK_1 | 273 | 279 | PF00454 | 0.750 |
MOD_PKA_1 | 217 | 223 | PF00069 | 0.534 |
MOD_PKA_2 | 10 | 16 | PF00069 | 0.558 |
MOD_PKA_2 | 150 | 156 | PF00069 | 0.772 |
MOD_PKA_2 | 160 | 166 | PF00069 | 0.677 |
MOD_PKA_2 | 171 | 177 | PF00069 | 0.617 |
MOD_PKA_2 | 299 | 305 | PF00069 | 0.721 |
MOD_PKA_2 | 336 | 342 | PF00069 | 0.692 |
MOD_Plk_1 | 20 | 26 | PF00069 | 0.683 |
MOD_Plk_1 | 284 | 290 | PF00069 | 0.558 |
MOD_Plk_1 | 394 | 400 | PF00069 | 0.647 |
MOD_Plk_4 | 26 | 32 | PF00069 | 0.565 |
MOD_ProDKin_1 | 143 | 149 | PF00069 | 0.717 |
MOD_ProDKin_1 | 165 | 171 | PF00069 | 0.693 |
MOD_ProDKin_1 | 247 | 253 | PF00069 | 0.564 |
MOD_ProDKin_1 | 370 | 376 | PF00069 | 0.665 |
MOD_SUMO_rev_2 | 434 | 442 | PF00179 | 0.609 |
MOD_SUMO_rev_2 | 79 | 89 | PF00179 | 0.626 |
TRG_DiLeu_BaEn_4 | 124 | 130 | PF01217 | 0.668 |
TRG_ER_diArg_1 | 98 | 101 | PF00400 | 0.498 |
TRG_NLS_MonoExtC_3 | 216 | 221 | PF00514 | 0.574 |
TRG_Pf-PMV_PEXEL_1 | 187 | 191 | PF00026 | 0.551 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PE29 | Leptomonas seymouri | 67% | 99% |
A0A1X0P7K1 | Trypanosomatidae | 36% | 100% |
A0A3Q8ICW8 | Leishmania donovani | 96% | 100% |
A0A3R7NTG2 | Trypanosoma rangeli | 35% | 100% |
A4HK15 | Leishmania braziliensis | 82% | 100% |
A4I7J9 | Leishmania infantum | 96% | 100% |
D0A0A1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
E9B2F6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
V5BS76 | Trypanosoma cruzi | 35% | 100% |