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: Q4QG92
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 119 | 121 | PF00675 | 0.707 |
CLV_NRD_NRD_1 | 182 | 184 | PF00675 | 0.646 |
CLV_NRD_NRD_1 | 276 | 278 | PF00675 | 0.484 |
CLV_NRD_NRD_1 | 306 | 308 | PF00675 | 0.443 |
CLV_NRD_NRD_1 | 313 | 315 | PF00675 | 0.439 |
CLV_NRD_NRD_1 | 339 | 341 | PF00675 | 0.426 |
CLV_NRD_NRD_1 | 382 | 384 | PF00675 | 0.439 |
CLV_NRD_NRD_1 | 395 | 397 | PF00675 | 0.425 |
CLV_NRD_NRD_1 | 73 | 75 | PF00675 | 0.644 |
CLV_PCSK_KEX2_1 | 119 | 121 | PF00082 | 0.707 |
CLV_PCSK_KEX2_1 | 276 | 278 | PF00082 | 0.484 |
CLV_PCSK_KEX2_1 | 306 | 308 | PF00082 | 0.443 |
CLV_PCSK_KEX2_1 | 313 | 315 | PF00082 | 0.439 |
CLV_PCSK_KEX2_1 | 339 | 341 | PF00082 | 0.394 |
CLV_PCSK_SKI1_1 | 313 | 317 | PF00082 | 0.438 |
CLV_PCSK_SKI1_1 | 343 | 347 | PF00082 | 0.426 |
CLV_PCSK_SKI1_1 | 383 | 387 | PF00082 | 0.516 |
CLV_PCSK_SKI1_1 | 410 | 414 | PF00082 | 0.435 |
DEG_APCC_DBOX_1 | 409 | 417 | PF00400 | 0.414 |
DEG_SCF_FBW7_1 | 212 | 217 | PF00400 | 0.699 |
DEG_SCF_FBW7_1 | 35 | 42 | PF00400 | 0.653 |
DEG_SCF_FBW7_1 | 99 | 105 | PF00400 | 0.566 |
DEG_SPOP_SBC_1 | 132 | 136 | PF00917 | 0.650 |
DEG_SPOP_SBC_1 | 154 | 158 | PF00917 | 0.822 |
DEG_SPOP_SBC_1 | 252 | 256 | PF00917 | 0.634 |
DEG_SPOP_SBC_1 | 59 | 63 | PF00917 | 0.619 |
DEG_SPOP_SBC_1 | 86 | 90 | PF00917 | 0.677 |
DEG_SPOP_SBC_1 | 92 | 96 | PF00917 | 0.612 |
DOC_CKS1_1 | 20 | 25 | PF01111 | 0.583 |
DOC_CKS1_1 | 211 | 216 | PF01111 | 0.703 |
DOC_CKS1_1 | 36 | 41 | PF01111 | 0.654 |
DOC_CKS1_1 | 99 | 104 | PF01111 | 0.565 |
DOC_MAPK_DCC_7 | 414 | 422 | PF00069 | 0.509 |
DOC_MAPK_MEF2A_6 | 414 | 422 | PF00069 | 0.509 |
DOC_USP7_MATH_1 | 102 | 106 | PF00917 | 0.468 |
DOC_USP7_MATH_1 | 109 | 113 | PF00917 | 0.628 |
DOC_USP7_MATH_1 | 132 | 136 | PF00917 | 0.672 |
DOC_USP7_MATH_1 | 154 | 158 | PF00917 | 0.648 |
DOC_USP7_MATH_1 | 230 | 234 | PF00917 | 0.716 |
DOC_USP7_MATH_1 | 252 | 256 | PF00917 | 0.619 |
DOC_USP7_MATH_1 | 59 | 63 | PF00917 | 0.619 |
DOC_USP7_MATH_1 | 86 | 90 | PF00917 | 0.777 |
DOC_USP7_MATH_1 | 92 | 96 | PF00917 | 0.717 |
DOC_WW_Pin1_4 | 128 | 133 | PF00397 | 0.754 |
DOC_WW_Pin1_4 | 147 | 152 | PF00397 | 0.664 |
DOC_WW_Pin1_4 | 155 | 160 | PF00397 | 0.786 |
DOC_WW_Pin1_4 | 172 | 177 | PF00397 | 0.523 |
DOC_WW_Pin1_4 | 19 | 24 | PF00397 | 0.543 |
DOC_WW_Pin1_4 | 210 | 215 | PF00397 | 0.675 |
DOC_WW_Pin1_4 | 28 | 33 | PF00397 | 0.535 |
DOC_WW_Pin1_4 | 35 | 40 | PF00397 | 0.598 |
DOC_WW_Pin1_4 | 98 | 103 | PF00397 | 0.574 |
LIG_14-3-3_CanoR_1 | 306 | 315 | PF00244 | 0.438 |
LIG_14-3-3_CanoR_1 | 340 | 346 | PF00244 | 0.360 |
LIG_14-3-3_CanoR_1 | 383 | 392 | PF00244 | 0.508 |
LIG_APCC_ABBA_1 | 315 | 320 | PF00400 | 0.442 |
LIG_APCC_ABBAyCdc20_2 | 314 | 320 | PF00400 | 0.442 |
LIG_BRCT_BRCA1_1 | 23 | 27 | PF00533 | 0.616 |
LIG_EH_1 | 47 | 51 | PF12763 | 0.664 |
LIG_FHA_1 | 136 | 142 | PF00498 | 0.611 |
LIG_FHA_1 | 292 | 298 | PF00498 | 0.492 |
LIG_FHA_1 | 40 | 46 | PF00498 | 0.659 |
LIG_FHA_1 | 79 | 85 | PF00498 | 0.695 |
LIG_FHA_1 | 94 | 100 | PF00498 | 0.522 |
LIG_FHA_2 | 321 | 327 | PF00498 | 0.472 |
LIG_LIR_Apic_2 | 208 | 214 | PF02991 | 0.633 |
LIG_LIR_Gen_1 | 9 | 19 | PF02991 | 0.721 |
LIG_LIR_Nem_3 | 9 | 14 | PF02991 | 0.745 |
LIG_LYPXL_yS_3 | 18 | 21 | PF13949 | 0.609 |
LIG_PCNA_yPIPBox_3 | 354 | 364 | PF02747 | 0.408 |
LIG_SH2_CRK | 11 | 15 | PF00017 | 0.674 |
LIG_SH2_CRK | 190 | 194 | PF00017 | 0.504 |
LIG_SH2_CRK | 225 | 229 | PF00017 | 0.697 |
LIG_SH3_3 | 148 | 154 | PF00018 | 0.663 |
LIG_SH3_3 | 213 | 219 | PF00018 | 0.705 |
LIG_SH3_3 | 267 | 273 | PF00018 | 0.518 |
LIG_SH3_3 | 46 | 52 | PF00018 | 0.585 |
LIG_SUMO_SIM_anti_2 | 390 | 396 | PF11976 | 0.432 |
LIG_SUMO_SIM_par_1 | 94 | 101 | PF11976 | 0.596 |
LIG_TRAF2_1 | 324 | 327 | PF00917 | 0.445 |
LIG_TRAF2_1 | 335 | 338 | PF00917 | 0.429 |
LIG_TYR_ITIM | 188 | 193 | PF00017 | 0.450 |
LIG_TYR_ITIM | 223 | 228 | PF00017 | 0.655 |
MOD_CK1_1 | 105 | 111 | PF00069 | 0.579 |
MOD_CK1_1 | 130 | 136 | PF00069 | 0.605 |
MOD_CK1_1 | 217 | 223 | PF00069 | 0.660 |
MOD_CK1_1 | 255 | 261 | PF00069 | 0.623 |
MOD_CK1_1 | 282 | 288 | PF00069 | 0.531 |
MOD_CK1_1 | 58 | 64 | PF00069 | 0.783 |
MOD_CK1_1 | 73 | 79 | PF00069 | 0.585 |
MOD_CK1_1 | 82 | 88 | PF00069 | 0.631 |
MOD_CK1_1 | 95 | 101 | PF00069 | 0.738 |
MOD_CK2_1 | 320 | 326 | PF00069 | 0.489 |
MOD_Cter_Amidation | 311 | 314 | PF01082 | 0.442 |
MOD_GlcNHglycan | 107 | 110 | PF01048 | 0.667 |
MOD_GlcNHglycan | 111 | 114 | PF01048 | 0.648 |
MOD_GlcNHglycan | 219 | 222 | PF01048 | 0.608 |
MOD_GlcNHglycan | 230 | 233 | PF01048 | 0.690 |
MOD_GlcNHglycan | 242 | 245 | PF01048 | 0.543 |
MOD_GlcNHglycan | 289 | 292 | PF01048 | 0.603 |
MOD_GlcNHglycan | 331 | 335 | PF01048 | 0.377 |
MOD_GlcNHglycan | 404 | 409 | PF01048 | 0.448 |
MOD_GlcNHglycan | 57 | 60 | PF01048 | 0.672 |
MOD_GlcNHglycan | 81 | 84 | PF01048 | 0.749 |
MOD_GlcNHglycan | 89 | 92 | PF01048 | 0.723 |
MOD_GSK3_1 | 105 | 112 | PF00069 | 0.554 |
MOD_GSK3_1 | 127 | 134 | PF00069 | 0.774 |
MOD_GSK3_1 | 155 | 162 | PF00069 | 0.779 |
MOD_GSK3_1 | 210 | 217 | PF00069 | 0.687 |
MOD_GSK3_1 | 236 | 243 | PF00069 | 0.802 |
MOD_GSK3_1 | 247 | 254 | PF00069 | 0.586 |
MOD_GSK3_1 | 279 | 286 | PF00069 | 0.562 |
MOD_GSK3_1 | 287 | 294 | PF00069 | 0.526 |
MOD_GSK3_1 | 341 | 348 | PF00069 | 0.406 |
MOD_GSK3_1 | 35 | 42 | PF00069 | 0.668 |
MOD_GSK3_1 | 55 | 62 | PF00069 | 0.492 |
MOD_GSK3_1 | 75 | 82 | PF00069 | 0.526 |
MOD_GSK3_1 | 87 | 94 | PF00069 | 0.587 |
MOD_GSK3_1 | 97 | 104 | PF00069 | 0.523 |
MOD_N-GLC_1 | 55 | 60 | PF02516 | 0.601 |
MOD_NEK2_1 | 253 | 258 | PF00069 | 0.650 |
MOD_NEK2_1 | 308 | 313 | PF00069 | 0.439 |
MOD_NEK2_1 | 341 | 346 | PF00069 | 0.428 |
MOD_NEK2_1 | 93 | 98 | PF00069 | 0.605 |
MOD_PKA_1 | 119 | 125 | PF00069 | 0.709 |
MOD_PKA_1 | 383 | 389 | PF00069 | 0.487 |
MOD_PKA_2 | 119 | 125 | PF00069 | 0.689 |
MOD_PKA_2 | 390 | 396 | PF00069 | 0.452 |
MOD_PKA_2 | 73 | 79 | PF00069 | 0.747 |
MOD_PKB_1 | 77 | 85 | PF00069 | 0.573 |
MOD_Plk_4 | 390 | 396 | PF00069 | 0.503 |
MOD_ProDKin_1 | 128 | 134 | PF00069 | 0.753 |
MOD_ProDKin_1 | 147 | 153 | PF00069 | 0.660 |
MOD_ProDKin_1 | 155 | 161 | PF00069 | 0.786 |
MOD_ProDKin_1 | 172 | 178 | PF00069 | 0.524 |
MOD_ProDKin_1 | 19 | 25 | PF00069 | 0.543 |
MOD_ProDKin_1 | 210 | 216 | PF00069 | 0.673 |
MOD_ProDKin_1 | 28 | 34 | PF00069 | 0.529 |
MOD_ProDKin_1 | 35 | 41 | PF00069 | 0.602 |
MOD_ProDKin_1 | 98 | 104 | PF00069 | 0.575 |
TRG_DiLeu_BaEn_1 | 337 | 342 | PF01217 | 0.424 |
TRG_DiLeu_BaEn_4 | 327 | 333 | PF01217 | 0.533 |
TRG_DiLeu_BaLyEn_6 | 304 | 309 | PF01217 | 0.438 |
TRG_DiLeu_BaLyEn_6 | 49 | 54 | PF01217 | 0.585 |
TRG_ENDOCYTIC_2 | 11 | 14 | PF00928 | 0.632 |
TRG_ENDOCYTIC_2 | 18 | 21 | PF00928 | 0.555 |
TRG_ENDOCYTIC_2 | 190 | 193 | PF00928 | 0.482 |
TRG_ENDOCYTIC_2 | 225 | 228 | PF00928 | 0.704 |
TRG_ER_diArg_1 | 119 | 121 | PF00400 | 0.630 |
TRG_ER_diArg_1 | 275 | 277 | PF00400 | 0.474 |
TRG_ER_diArg_1 | 306 | 308 | PF00400 | 0.443 |
TRG_ER_diArg_1 | 313 | 315 | PF00400 | 0.439 |
TRG_ER_diArg_1 | 339 | 341 | PF00400 | 0.369 |
TRG_ER_diArg_1 | 77 | 80 | PF00400 | 0.571 |
TRG_Pf-PMV_PEXEL_1 | 277 | 281 | PF00026 | 0.475 |
TRG_Pf-PMV_PEXEL_1 | 364 | 368 | PF00026 | 0.421 |
TRG_Pf-PMV_PEXEL_1 | 383 | 387 | PF00026 | 0.440 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PEE7 | Leptomonas seymouri | 46% | 100% |
A0A3Q8I9J2 | Leishmania donovani | 90% | 100% |
A4H751 | Leishmania braziliensis | 74% | 100% |
A4HVJ1 | Leishmania infantum | 90% | 100% |
E9AP86 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |