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: 5 |
NetGPI | no | yes: 0, no: 5 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005929 | cilium | 4 | 6 |
GO:0042995 | cell projection | 2 | 6 |
GO:0043226 | organelle | 2 | 6 |
GO:0043227 | membrane-bounded organelle | 3 | 6 |
GO:0110165 | cellular anatomical entity | 1 | 6 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 6 |
Related structures:
AlphaFold database: Q4QC70
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 240 | 244 | PF00656 | 0.615 |
CLV_C14_Caspase3-7 | 328 | 332 | PF00656 | 0.561 |
CLV_C14_Caspase3-7 | 399 | 403 | PF00656 | 0.612 |
CLV_C14_Caspase3-7 | 421 | 425 | PF00656 | 0.639 |
CLV_NRD_NRD_1 | 201 | 203 | PF00675 | 0.502 |
CLV_NRD_NRD_1 | 205 | 207 | PF00675 | 0.492 |
CLV_NRD_NRD_1 | 213 | 215 | PF00675 | 0.503 |
CLV_NRD_NRD_1 | 379 | 381 | PF00675 | 0.631 |
CLV_NRD_NRD_1 | 97 | 99 | PF00675 | 0.385 |
CLV_PCSK_KEX2_1 | 201 | 203 | PF00082 | 0.502 |
CLV_PCSK_KEX2_1 | 205 | 207 | PF00082 | 0.492 |
CLV_PCSK_KEX2_1 | 213 | 215 | PF00082 | 0.503 |
CLV_PCSK_KEX2_1 | 379 | 381 | PF00082 | 0.631 |
CLV_PCSK_KEX2_1 | 97 | 99 | PF00082 | 0.385 |
CLV_PCSK_PC7_1 | 201 | 207 | PF00082 | 0.519 |
CLV_PCSK_SKI1_1 | 189 | 193 | PF00082 | 0.421 |
DEG_APCC_DBOX_1 | 188 | 196 | PF00400 | 0.416 |
DEG_APCC_DBOX_1 | 212 | 220 | PF00400 | 0.573 |
DEG_APCC_DBOX_1 | 62 | 70 | PF00400 | 0.441 |
DEG_SCF_TRCP1_1 | 346 | 351 | PF00400 | 0.553 |
DOC_CYCLIN_RxL_1 | 186 | 196 | PF00134 | 0.419 |
DOC_CYCLIN_RxL_1 | 79 | 90 | PF00134 | 0.404 |
DOC_USP7_MATH_1 | 228 | 232 | PF00917 | 0.655 |
DOC_USP7_MATH_1 | 391 | 395 | PF00917 | 0.611 |
DOC_USP7_MATH_1 | 420 | 424 | PF00917 | 0.611 |
DOC_USP7_MATH_1 | 431 | 435 | PF00917 | 0.611 |
DOC_WW_Pin1_4 | 233 | 238 | PF00397 | 0.637 |
DOC_WW_Pin1_4 | 264 | 269 | PF00397 | 0.622 |
DOC_WW_Pin1_4 | 351 | 356 | PF00397 | 0.649 |
DOC_WW_Pin1_4 | 412 | 417 | PF00397 | 0.661 |
LIG_14-3-3_CanoR_1 | 141 | 147 | PF00244 | 0.532 |
LIG_14-3-3_CanoR_1 | 206 | 216 | PF00244 | 0.537 |
LIG_14-3-3_CanoR_1 | 238 | 247 | PF00244 | 0.633 |
LIG_14-3-3_CanoR_1 | 404 | 412 | PF00244 | 0.611 |
LIG_14-3-3_CanoR_1 | 63 | 67 | PF00244 | 0.451 |
LIG_Actin_WH2_2 | 381 | 398 | PF00022 | 0.571 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.568 |
LIG_BRCT_BRCA1_1 | 422 | 426 | PF00533 | 0.590 |
LIG_BRCT_BRCA1_1 | 89 | 93 | PF00533 | 0.303 |
LIG_EVH1_1 | 450 | 454 | PF00568 | 0.622 |
LIG_FHA_1 | 42 | 48 | PF00498 | 0.413 |
LIG_FHA_1 | 66 | 72 | PF00498 | 0.399 |
LIG_FHA_2 | 419 | 425 | PF00498 | 0.651 |
LIG_LIR_Apic_2 | 448 | 453 | PF02991 | 0.620 |
LIG_LIR_Gen_1 | 90 | 101 | PF02991 | 0.318 |
LIG_LIR_Nem_3 | 174 | 178 | PF02991 | 0.424 |
LIG_LIR_Nem_3 | 423 | 429 | PF02991 | 0.650 |
LIG_LIR_Nem_3 | 90 | 96 | PF02991 | 0.368 |
LIG_PCNA_yPIPBox_3 | 26 | 40 | PF02747 | 0.336 |
LIG_PDZ_Class_3 | 495 | 500 | PF00595 | 0.616 |
LIG_Rb_LxCxE_1 | 157 | 174 | PF01857 | 0.451 |
LIG_SH2_NCK_1 | 326 | 330 | PF00017 | 0.596 |
LIG_SH2_PTP2 | 175 | 178 | PF00017 | 0.418 |
LIG_SH2_STAT3 | 369 | 372 | PF00017 | 0.568 |
LIG_SH2_STAT5 | 175 | 178 | PF00017 | 0.477 |
LIG_SH2_STAT5 | 326 | 329 | PF00017 | 0.576 |
LIG_SH2_STAT5 | 429 | 432 | PF00017 | 0.575 |
LIG_SH3_2 | 451 | 456 | PF14604 | 0.666 |
LIG_SH3_3 | 145 | 151 | PF00018 | 0.541 |
LIG_SH3_3 | 244 | 250 | PF00018 | 0.685 |
LIG_SH3_3 | 414 | 420 | PF00018 | 0.655 |
LIG_SH3_3 | 446 | 452 | PF00018 | 0.674 |
LIG_SH3_5 | 322 | 326 | PF00018 | 0.620 |
LIG_SUMO_SIM_par_1 | 2 | 10 | PF11976 | 0.456 |
LIG_SUMO_SIM_par_1 | 38 | 44 | PF11976 | 0.385 |
LIG_SUMO_SIM_par_1 | 67 | 72 | PF11976 | 0.392 |
LIG_TYR_ITIM | 173 | 178 | PF00017 | 0.423 |
MOD_CDK_SPK_2 | 233 | 238 | PF00069 | 0.626 |
MOD_CK1_1 | 142 | 148 | PF00069 | 0.615 |
MOD_CK1_1 | 351 | 357 | PF00069 | 0.623 |
MOD_CK1_1 | 41 | 47 | PF00069 | 0.321 |
MOD_CK1_1 | 72 | 78 | PF00069 | 0.375 |
MOD_CK2_1 | 380 | 386 | PF00069 | 0.637 |
MOD_CK2_1 | 391 | 397 | PF00069 | 0.640 |
MOD_GlcNHglycan | 141 | 144 | PF01048 | 0.626 |
MOD_GlcNHglycan | 21 | 24 | PF01048 | 0.535 |
MOD_GlcNHglycan | 223 | 226 | PF01048 | 0.630 |
MOD_GlcNHglycan | 229 | 233 | PF01048 | 0.619 |
MOD_GlcNHglycan | 240 | 243 | PF01048 | 0.509 |
MOD_GlcNHglycan | 327 | 330 | PF01048 | 0.656 |
MOD_GlcNHglycan | 333 | 336 | PF01048 | 0.619 |
MOD_GlcNHglycan | 345 | 349 | PF01048 | 0.516 |
MOD_GlcNHglycan | 364 | 367 | PF01048 | 0.604 |
MOD_GlcNHglycan | 380 | 383 | PF01048 | 0.708 |
MOD_GlcNHglycan | 397 | 401 | PF01048 | 0.507 |
MOD_GlcNHglycan | 432 | 436 | PF01048 | 0.682 |
MOD_GlcNHglycan | 477 | 480 | PF01048 | 0.699 |
MOD_GlcNHglycan | 89 | 92 | PF01048 | 0.385 |
MOD_GlcNHglycan | 93 | 96 | PF01048 | 0.356 |
MOD_GSK3_1 | 208 | 215 | PF00069 | 0.564 |
MOD_GSK3_1 | 233 | 240 | PF00069 | 0.640 |
MOD_GSK3_1 | 344 | 351 | PF00069 | 0.558 |
MOD_GSK3_1 | 407 | 414 | PF00069 | 0.603 |
MOD_GSK3_1 | 416 | 423 | PF00069 | 0.597 |
MOD_GSK3_1 | 427 | 434 | PF00069 | 0.511 |
MOD_GSK3_1 | 65 | 72 | PF00069 | 0.476 |
MOD_GSK3_1 | 87 | 94 | PF00069 | 0.380 |
MOD_LATS_1 | 378 | 384 | PF00433 | 0.678 |
MOD_N-GLC_1 | 331 | 336 | PF02516 | 0.547 |
MOD_N-GLC_1 | 391 | 396 | PF02516 | 0.599 |
MOD_N-GLC_1 | 77 | 82 | PF02516 | 0.391 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.495 |
MOD_NEK2_1 | 207 | 212 | PF00069 | 0.500 |
MOD_NEK2_1 | 40 | 45 | PF00069 | 0.437 |
MOD_NEK2_1 | 69 | 74 | PF00069 | 0.497 |
MOD_NEK2_2 | 120 | 125 | PF00069 | 0.494 |
MOD_NEK2_2 | 391 | 396 | PF00069 | 0.573 |
MOD_NEK2_2 | 62 | 67 | PF00069 | 0.444 |
MOD_PIKK_1 | 208 | 214 | PF00454 | 0.562 |
MOD_PK_1 | 380 | 386 | PF00069 | 0.636 |
MOD_PKA_2 | 193 | 199 | PF00069 | 0.434 |
MOD_PKA_2 | 212 | 218 | PF00069 | 0.468 |
MOD_PKA_2 | 221 | 227 | PF00069 | 0.526 |
MOD_PKA_2 | 237 | 243 | PF00069 | 0.516 |
MOD_PKA_2 | 301 | 307 | PF00069 | 0.629 |
MOD_PKA_2 | 378 | 384 | PF00069 | 0.747 |
MOD_PKA_2 | 62 | 68 | PF00069 | 0.444 |
MOD_Plk_1 | 178 | 184 | PF00069 | 0.560 |
MOD_Plk_1 | 391 | 397 | PF00069 | 0.573 |
MOD_Plk_1 | 77 | 83 | PF00069 | 0.394 |
MOD_Plk_2-3 | 270 | 276 | PF00069 | 0.548 |
MOD_Plk_4 | 1 | 7 | PF00069 | 0.488 |
MOD_Plk_4 | 154 | 160 | PF00069 | 0.464 |
MOD_Plk_4 | 359 | 365 | PF00069 | 0.701 |
MOD_ProDKin_1 | 233 | 239 | PF00069 | 0.637 |
MOD_ProDKin_1 | 264 | 270 | PF00069 | 0.623 |
MOD_ProDKin_1 | 351 | 357 | PF00069 | 0.650 |
MOD_ProDKin_1 | 412 | 418 | PF00069 | 0.660 |
TRG_DiLeu_BaEn_1 | 32 | 37 | PF01217 | 0.373 |
TRG_ENDOCYTIC_2 | 175 | 178 | PF00928 | 0.418 |
TRG_ER_diArg_1 | 205 | 207 | PF00400 | 0.514 |
TRG_ER_diArg_1 | 96 | 98 | PF00400 | 0.385 |
TRG_Pf-PMV_PEXEL_1 | 189 | 193 | PF00026 | 0.443 |
TRG_Pf-PMV_PEXEL_1 | 308 | 312 | PF00026 | 0.535 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7WWT1 | Leishmania donovani | 84% | 100% |
A4HBY1 | Leishmania braziliensis | 54% | 100% |
A4HZC3 | Leishmania infantum | 85% | 100% |
E9AVB0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 77% | 100% |