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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005815 | microtubule organizing center | 2 | 2 |
GO:0036064 | ciliary basal body | 3 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4Q0B7
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 239 | 243 | PF00656 | 0.801 |
CLV_C14_Caspase3-7 | 319 | 323 | PF00656 | 0.570 |
CLV_NRD_NRD_1 | 187 | 189 | PF00675 | 0.529 |
CLV_NRD_NRD_1 | 271 | 273 | PF00675 | 0.608 |
CLV_NRD_NRD_1 | 286 | 288 | PF00675 | 0.591 |
CLV_NRD_NRD_1 | 294 | 296 | PF00675 | 0.563 |
CLV_NRD_NRD_1 | 329 | 331 | PF00675 | 0.779 |
CLV_NRD_NRD_1 | 416 | 418 | PF00675 | 0.714 |
CLV_NRD_NRD_1 | 438 | 440 | PF00675 | 0.689 |
CLV_NRD_NRD_1 | 46 | 48 | PF00675 | 0.464 |
CLV_NRD_NRD_1 | 509 | 511 | PF00675 | 0.752 |
CLV_NRD_NRD_1 | 81 | 83 | PF00675 | 0.471 |
CLV_PCSK_KEX2_1 | 204 | 206 | PF00082 | 0.574 |
CLV_PCSK_KEX2_1 | 271 | 273 | PF00082 | 0.615 |
CLV_PCSK_KEX2_1 | 286 | 288 | PF00082 | 0.597 |
CLV_PCSK_KEX2_1 | 294 | 296 | PF00082 | 0.567 |
CLV_PCSK_KEX2_1 | 329 | 331 | PF00082 | 0.779 |
CLV_PCSK_KEX2_1 | 438 | 440 | PF00082 | 0.689 |
CLV_PCSK_KEX2_1 | 46 | 48 | PF00082 | 0.464 |
CLV_PCSK_KEX2_1 | 511 | 513 | PF00082 | 0.684 |
CLV_PCSK_PC1ET2_1 | 204 | 206 | PF00082 | 0.606 |
CLV_PCSK_PC1ET2_1 | 511 | 513 | PF00082 | 0.684 |
CLV_PCSK_PC7_1 | 434 | 440 | PF00082 | 0.686 |
CLV_PCSK_PC7_1 | 507 | 513 | PF00082 | 0.691 |
CLV_PCSK_SKI1_1 | 137 | 141 | PF00082 | 0.411 |
CLV_PCSK_SKI1_1 | 169 | 173 | PF00082 | 0.375 |
CLV_PCSK_SKI1_1 | 248 | 252 | PF00082 | 0.691 |
CLV_PCSK_SKI1_1 | 26 | 30 | PF00082 | 0.530 |
CLV_PCSK_SKI1_1 | 46 | 50 | PF00082 | 0.411 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.542 |
DEG_SPOP_SBC_1 | 206 | 210 | PF00917 | 0.630 |
DOC_ANK_TNKS_1 | 106 | 113 | PF00023 | 0.676 |
DOC_CYCLIN_RxL_1 | 148 | 156 | PF00134 | 0.403 |
DOC_CYCLIN_RxL_1 | 43 | 53 | PF00134 | 0.461 |
DOC_MAPK_gen_1 | 149 | 157 | PF00069 | 0.502 |
DOC_MAPK_gen_1 | 166 | 172 | PF00069 | 0.221 |
DOC_MAPK_gen_1 | 329 | 335 | PF00069 | 0.574 |
DOC_MAPK_gen_1 | 80 | 90 | PF00069 | 0.565 |
DOC_MAPK_MEF2A_6 | 149 | 157 | PF00069 | 0.408 |
DOC_MAPK_MEF2A_6 | 166 | 174 | PF00069 | 0.247 |
DOC_MAPK_MEF2A_6 | 36 | 43 | PF00069 | 0.446 |
DOC_MAPK_RevD_3 | 153 | 167 | PF00069 | 0.513 |
DOC_PP1_RVXF_1 | 80 | 87 | PF00149 | 0.464 |
DOC_PP2B_LxvP_1 | 155 | 158 | PF13499 | 0.411 |
DOC_PP2B_LxvP_1 | 333 | 336 | PF13499 | 0.658 |
DOC_PP4_FxxP_1 | 432 | 435 | PF00568 | 0.703 |
DOC_USP7_MATH_1 | 213 | 217 | PF00917 | 0.628 |
DOC_USP7_MATH_1 | 222 | 226 | PF00917 | 0.574 |
DOC_USP7_MATH_1 | 254 | 258 | PF00917 | 0.657 |
DOC_USP7_MATH_1 | 274 | 278 | PF00917 | 0.374 |
DOC_USP7_MATH_1 | 334 | 338 | PF00917 | 0.692 |
DOC_USP7_MATH_1 | 359 | 363 | PF00917 | 0.728 |
DOC_USP7_MATH_1 | 495 | 499 | PF00917 | 0.569 |
DOC_USP7_MATH_2 | 455 | 461 | PF00917 | 0.802 |
DOC_WW_Pin1_4 | 252 | 257 | PF00397 | 0.664 |
DOC_WW_Pin1_4 | 469 | 474 | PF00397 | 0.800 |
LIG_14-3-3_CanoR_1 | 115 | 119 | PF00244 | 0.411 |
LIG_14-3-3_CanoR_1 | 130 | 140 | PF00244 | 0.411 |
LIG_14-3-3_CanoR_1 | 229 | 233 | PF00244 | 0.726 |
LIG_14-3-3_CanoR_1 | 271 | 280 | PF00244 | 0.587 |
LIG_14-3-3_CanoR_1 | 368 | 377 | PF00244 | 0.784 |
LIG_14-3-3_CanoR_1 | 438 | 442 | PF00244 | 0.686 |
LIG_14-3-3_CanoR_1 | 497 | 503 | PF00244 | 0.678 |
LIG_14-3-3_CanoR_1 | 5 | 14 | PF00244 | 0.502 |
LIG_BIR_III_2 | 305 | 309 | PF00653 | 0.537 |
LIG_BRCT_BRCA1_1 | 210 | 214 | PF00533 | 0.686 |
LIG_BRCT_BRCA1_1 | 514 | 518 | PF00533 | 0.580 |
LIG_FHA_1 | 222 | 228 | PF00498 | 0.776 |
LIG_FHA_1 | 353 | 359 | PF00498 | 0.677 |
LIG_FHA_1 | 466 | 472 | PF00498 | 0.607 |
LIG_FHA_1 | 478 | 484 | PF00498 | 0.713 |
LIG_FHA_1 | 487 | 493 | PF00498 | 0.598 |
LIG_FHA_1 | 7 | 13 | PF00498 | 0.462 |
LIG_FHA_1 | 79 | 85 | PF00498 | 0.472 |
LIG_FHA_1 | 98 | 104 | PF00498 | 0.520 |
LIG_FHA_2 | 237 | 243 | PF00498 | 0.800 |
LIG_FHA_2 | 317 | 323 | PF00498 | 0.573 |
LIG_FHA_2 | 438 | 444 | PF00498 | 0.703 |
LIG_FHA_2 | 499 | 505 | PF00498 | 0.648 |
LIG_IBAR_NPY_1 | 77 | 79 | PF08397 | 0.601 |
LIG_LIR_Apic_2 | 429 | 435 | PF02991 | 0.692 |
LIG_LIR_Apic_2 | 449 | 455 | PF02991 | 0.449 |
LIG_LIR_Gen_1 | 111 | 121 | PF02991 | 0.513 |
LIG_LIR_Gen_1 | 138 | 147 | PF02991 | 0.411 |
LIG_LIR_Gen_1 | 197 | 206 | PF02991 | 0.655 |
LIG_LIR_Gen_1 | 341 | 352 | PF02991 | 0.705 |
LIG_LIR_Gen_1 | 35 | 45 | PF02991 | 0.445 |
LIG_LIR_Gen_1 | 501 | 508 | PF02991 | 0.556 |
LIG_LIR_Gen_1 | 65 | 73 | PF02991 | 0.489 |
LIG_LIR_Nem_3 | 111 | 116 | PF02991 | 0.631 |
LIG_LIR_Nem_3 | 138 | 143 | PF02991 | 0.355 |
LIG_LIR_Nem_3 | 197 | 202 | PF02991 | 0.637 |
LIG_LIR_Nem_3 | 231 | 235 | PF02991 | 0.559 |
LIG_LIR_Nem_3 | 341 | 347 | PF02991 | 0.702 |
LIG_LIR_Nem_3 | 35 | 41 | PF02991 | 0.390 |
LIG_LIR_Nem_3 | 501 | 505 | PF02991 | 0.552 |
LIG_LIR_Nem_3 | 65 | 71 | PF02991 | 0.483 |
LIG_Pex14_1 | 64 | 68 | PF04695 | 0.474 |
LIG_Pex14_2 | 60 | 64 | PF04695 | 0.432 |
LIG_SH2_CRK | 344 | 348 | PF00017 | 0.685 |
LIG_SH2_CRK | 452 | 456 | PF00017 | 0.688 |
LIG_SH2_GRB2like | 92 | 95 | PF00017 | 0.577 |
LIG_SH2_NCK_1 | 315 | 319 | PF00017 | 0.772 |
LIG_SH2_NCK_1 | 344 | 348 | PF00017 | 0.809 |
LIG_SH2_NCK_1 | 452 | 456 | PF00017 | 0.688 |
LIG_SH2_PTP2 | 113 | 116 | PF00017 | 0.411 |
LIG_SH2_PTP2 | 68 | 71 | PF00017 | 0.481 |
LIG_SH2_SRC | 344 | 347 | PF00017 | 0.577 |
LIG_SH2_SRC | 502 | 505 | PF00017 | 0.553 |
LIG_SH2_STAP1 | 502 | 506 | PF00017 | 0.555 |
LIG_SH2_STAP1 | 92 | 96 | PF00017 | 0.470 |
LIG_SH2_STAT5 | 113 | 116 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 142 | 145 | PF00017 | 0.353 |
LIG_SH2_STAT5 | 315 | 318 | PF00017 | 0.698 |
LIG_SH2_STAT5 | 68 | 71 | PF00017 | 0.478 |
LIG_SH3_3 | 328 | 334 | PF00018 | 0.810 |
LIG_SH3_3 | 403 | 409 | PF00018 | 0.773 |
LIG_SUMO_SIM_anti_2 | 390 | 395 | PF11976 | 0.725 |
LIG_SUMO_SIM_par_1 | 392 | 401 | PF11976 | 0.826 |
LIG_TRAF2_1 | 265 | 268 | PF00917 | 0.587 |
LIG_UBA3_1 | 30 | 36 | PF00899 | 0.478 |
MOD_CDK_SPxxK_3 | 252 | 259 | PF00069 | 0.659 |
MOD_CK1_1 | 212 | 218 | PF00069 | 0.627 |
MOD_CK1_1 | 220 | 226 | PF00069 | 0.601 |
MOD_CK1_1 | 228 | 234 | PF00069 | 0.611 |
MOD_CK1_1 | 24 | 30 | PF00069 | 0.529 |
MOD_CK1_1 | 339 | 345 | PF00069 | 0.692 |
MOD_CK1_1 | 372 | 378 | PF00069 | 0.833 |
MOD_CK1_1 | 437 | 443 | PF00069 | 0.682 |
MOD_CK1_1 | 465 | 471 | PF00069 | 0.724 |
MOD_CK1_1 | 472 | 478 | PF00069 | 0.662 |
MOD_CK1_1 | 482 | 488 | PF00069 | 0.651 |
MOD_CK1_1 | 498 | 504 | PF00069 | 0.595 |
MOD_CK2_1 | 29 | 35 | PF00069 | 0.472 |
MOD_CK2_1 | 437 | 443 | PF00069 | 0.704 |
MOD_Cter_Amidation | 508 | 511 | PF01082 | 0.693 |
MOD_GlcNHglycan | 211 | 214 | PF01048 | 0.614 |
MOD_GlcNHglycan | 215 | 218 | PF01048 | 0.622 |
MOD_GlcNHglycan | 256 | 259 | PF01048 | 0.739 |
MOD_GlcNHglycan | 276 | 279 | PF01048 | 0.364 |
MOD_GlcNHglycan | 336 | 339 | PF01048 | 0.691 |
MOD_GlcNHglycan | 371 | 374 | PF01048 | 0.769 |
MOD_GlcNHglycan | 443 | 447 | PF01048 | 0.761 |
MOD_GlcNHglycan | 464 | 467 | PF01048 | 0.739 |
MOD_GlcNHglycan | 484 | 488 | PF01048 | 0.690 |
MOD_GlcNHglycan | 497 | 500 | PF01048 | 0.583 |
MOD_GlcNHglycan | 51 | 55 | PF01048 | 0.476 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.434 |
MOD_GSK3_1 | 205 | 212 | PF00069 | 0.579 |
MOD_GSK3_1 | 213 | 220 | PF00069 | 0.602 |
MOD_GSK3_1 | 221 | 228 | PF00069 | 0.582 |
MOD_GSK3_1 | 371 | 378 | PF00069 | 0.800 |
MOD_GSK3_1 | 430 | 437 | PF00069 | 0.691 |
MOD_GSK3_1 | 465 | 472 | PF00069 | 0.740 |
MOD_GSK3_1 | 479 | 486 | PF00069 | 0.811 |
MOD_N-GLC_1 | 21 | 26 | PF02516 | 0.624 |
MOD_N-GLC_1 | 313 | 318 | PF02516 | 0.614 |
MOD_N-GLC_1 | 359 | 364 | PF02516 | 0.609 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.533 |
MOD_NEK2_1 | 153 | 158 | PF00069 | 0.408 |
MOD_NEK2_1 | 450 | 455 | PF00069 | 0.676 |
MOD_NEK2_1 | 50 | 55 | PF00069 | 0.535 |
MOD_NEK2_2 | 161 | 166 | PF00069 | 0.513 |
MOD_PIKK_1 | 359 | 365 | PF00454 | 0.592 |
MOD_PIKK_1 | 450 | 456 | PF00454 | 0.682 |
MOD_PKA_1 | 272 | 278 | PF00069 | 0.581 |
MOD_PKA_2 | 114 | 120 | PF00069 | 0.408 |
MOD_PKA_2 | 220 | 226 | PF00069 | 0.670 |
MOD_PKA_2 | 228 | 234 | PF00069 | 0.691 |
MOD_PKA_2 | 352 | 358 | PF00069 | 0.830 |
MOD_PKA_2 | 437 | 443 | PF00069 | 0.682 |
MOD_PKB_1 | 510 | 518 | PF00069 | 0.705 |
MOD_Plk_1 | 24 | 30 | PF00069 | 0.550 |
MOD_Plk_4 | 24 | 30 | PF00069 | 0.529 |
MOD_Plk_4 | 339 | 345 | PF00069 | 0.692 |
MOD_Plk_4 | 522 | 528 | PF00069 | 0.677 |
MOD_ProDKin_1 | 252 | 258 | PF00069 | 0.664 |
MOD_ProDKin_1 | 469 | 475 | PF00069 | 0.798 |
MOD_SUMO_rev_2 | 242 | 249 | PF00179 | 0.685 |
TRG_DiLeu_BaEn_1 | 66 | 71 | PF01217 | 0.464 |
TRG_DiLeu_BaEn_4 | 66 | 72 | PF01217 | 0.471 |
TRG_DiLeu_BaLyEn_6 | 44 | 49 | PF01217 | 0.444 |
TRG_ENDOCYTIC_2 | 113 | 116 | PF00928 | 0.369 |
TRG_ENDOCYTIC_2 | 199 | 202 | PF00928 | 0.643 |
TRG_ENDOCYTIC_2 | 344 | 347 | PF00928 | 0.708 |
TRG_ENDOCYTIC_2 | 502 | 505 | PF00928 | 0.553 |
TRG_ENDOCYTIC_2 | 68 | 71 | PF00928 | 0.481 |
TRG_ER_diArg_1 | 149 | 152 | PF00400 | 0.389 |
TRG_ER_diArg_1 | 285 | 287 | PF00400 | 0.526 |
TRG_ER_diArg_1 | 294 | 296 | PF00400 | 0.567 |
TRG_ER_diArg_1 | 328 | 330 | PF00400 | 0.781 |
TRG_ER_diArg_1 | 46 | 48 | PF00400 | 0.464 |
TRG_ER_diArg_1 | 510 | 513 | PF00400 | 0.689 |
TRG_Pf-PMV_PEXEL_1 | 286 | 290 | PF00026 | 0.598 |
TRG_Pf-PMV_PEXEL_1 | 424 | 428 | PF00026 | 0.715 |
TRG_Pf-PMV_PEXEL_1 | 46 | 51 | PF00026 | 0.463 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I476 | Leptomonas seymouri | 57% | 94% |
A0A3Q8IPX9 | Leishmania donovani | 92% | 100% |
A4HQG1 | Leishmania braziliensis | 76% | 97% |
A4IC97 | Leishmania infantum | 92% | 100% |
E9AU77 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |