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:0005815 | microtubule organizing center | 2 | 2 |
GO:0036064 | ciliary basal body | 3 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4QH07
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 117 | 119 | PF00675 | 0.678 |
CLV_NRD_NRD_1 | 194 | 196 | PF00675 | 0.594 |
CLV_NRD_NRD_1 | 285 | 287 | PF00675 | 0.489 |
CLV_NRD_NRD_1 | 349 | 351 | PF00675 | 0.419 |
CLV_NRD_NRD_1 | 381 | 383 | PF00675 | 0.446 |
CLV_NRD_NRD_1 | 417 | 419 | PF00675 | 0.486 |
CLV_NRD_NRD_1 | 446 | 448 | PF00675 | 0.575 |
CLV_NRD_NRD_1 | 97 | 99 | PF00675 | 0.522 |
CLV_PCSK_FUR_1 | 95 | 99 | PF00082 | 0.451 |
CLV_PCSK_KEX2_1 | 116 | 118 | PF00082 | 0.706 |
CLV_PCSK_KEX2_1 | 194 | 196 | PF00082 | 0.594 |
CLV_PCSK_KEX2_1 | 285 | 287 | PF00082 | 0.415 |
CLV_PCSK_KEX2_1 | 348 | 350 | PF00082 | 0.419 |
CLV_PCSK_KEX2_1 | 381 | 383 | PF00082 | 0.446 |
CLV_PCSK_KEX2_1 | 416 | 418 | PF00082 | 0.438 |
CLV_PCSK_KEX2_1 | 446 | 448 | PF00082 | 0.461 |
CLV_PCSK_KEX2_1 | 97 | 99 | PF00082 | 0.459 |
CLV_PCSK_PC7_1 | 442 | 448 | PF00082 | 0.448 |
CLV_PCSK_PC7_1 | 93 | 99 | PF00082 | 0.386 |
CLV_PCSK_SKI1_1 | 195 | 199 | PF00082 | 0.617 |
CLV_PCSK_SKI1_1 | 290 | 294 | PF00082 | 0.594 |
CLV_PCSK_SKI1_1 | 334 | 338 | PF00082 | 0.485 |
CLV_PCSK_SKI1_1 | 382 | 386 | PF00082 | 0.490 |
CLV_PCSK_SKI1_1 | 398 | 402 | PF00082 | 0.516 |
DEG_APCC_DBOX_1 | 437 | 445 | PF00400 | 0.517 |
DEG_APCC_DBOX_1 | 81 | 89 | PF00400 | 0.536 |
DEG_SPOP_SBC_1 | 110 | 114 | PF00917 | 0.559 |
DOC_CKS1_1 | 227 | 232 | PF01111 | 0.612 |
DOC_CYCLIN_yCln2_LP_2 | 218 | 224 | PF00134 | 0.694 |
DOC_MAPK_gen_1 | 47 | 57 | PF00069 | 0.555 |
DOC_MAPK_MEF2A_6 | 50 | 57 | PF00069 | 0.557 |
DOC_MAPK_NFAT4_5 | 50 | 58 | PF00069 | 0.557 |
DOC_PP1_RVXF_1 | 15 | 21 | PF00149 | 0.410 |
DOC_PP2B_LxvP_1 | 218 | 221 | PF13499 | 0.695 |
DOC_PP2B_LxvP_1 | 224 | 227 | PF13499 | 0.643 |
DOC_USP7_MATH_1 | 109 | 113 | PF00917 | 0.628 |
DOC_USP7_MATH_1 | 124 | 128 | PF00917 | 0.746 |
DOC_USP7_MATH_1 | 179 | 183 | PF00917 | 0.779 |
DOC_USP7_MATH_1 | 189 | 193 | PF00917 | 0.667 |
DOC_USP7_MATH_1 | 411 | 415 | PF00917 | 0.504 |
DOC_WW_Pin1_4 | 166 | 171 | PF00397 | 0.695 |
DOC_WW_Pin1_4 | 173 | 178 | PF00397 | 0.689 |
DOC_WW_Pin1_4 | 196 | 201 | PF00397 | 0.751 |
DOC_WW_Pin1_4 | 226 | 231 | PF00397 | 0.652 |
LIG_14-3-3_CanoR_1 | 116 | 121 | PF00244 | 0.649 |
LIG_14-3-3_CanoR_1 | 266 | 270 | PF00244 | 0.493 |
LIG_14-3-3_CanoR_1 | 273 | 283 | PF00244 | 0.507 |
LIG_14-3-3_CanoR_1 | 316 | 323 | PF00244 | 0.501 |
LIG_14-3-3_CanoR_1 | 438 | 442 | PF00244 | 0.471 |
LIG_Actin_WH2_2 | 319 | 336 | PF00022 | 0.510 |
LIG_BRCT_BRCA1_1 | 227 | 231 | PF00533 | 0.565 |
LIG_FHA_1 | 144 | 150 | PF00498 | 0.585 |
LIG_FHA_1 | 243 | 249 | PF00498 | 0.497 |
LIG_FHA_1 | 63 | 69 | PF00498 | 0.601 |
LIG_FHA_2 | 276 | 282 | PF00498 | 0.553 |
LIG_GBD_Chelix_1 | 401 | 409 | PF00786 | 0.457 |
LIG_LIR_Gen_1 | 26 | 35 | PF02991 | 0.480 |
LIG_LIR_Nem_3 | 26 | 32 | PF02991 | 0.479 |
LIG_LYPXL_yS_3 | 367 | 370 | PF13949 | 0.538 |
LIG_MYND_1 | 196 | 200 | PF01753 | 0.594 |
LIG_PTB_Apo_2 | 216 | 223 | PF02174 | 0.593 |
LIG_PTB_Phospho_1 | 216 | 222 | PF10480 | 0.589 |
LIG_SH2_STAP1 | 75 | 79 | PF00017 | 0.554 |
LIG_SH2_STAT3 | 222 | 225 | PF00017 | 0.617 |
LIG_SH2_STAT3 | 75 | 78 | PF00017 | 0.436 |
LIG_SH2_STAT5 | 29 | 32 | PF00017 | 0.486 |
LIG_SH2_STAT5 | 294 | 297 | PF00017 | 0.454 |
LIG_SH3_3 | 224 | 230 | PF00018 | 0.607 |
LIG_SUMO_SIM_anti_2 | 299 | 308 | PF11976 | 0.445 |
LIG_SUMO_SIM_anti_2 | 432 | 438 | PF11976 | 0.464 |
LIG_SUMO_SIM_par_1 | 145 | 150 | PF11976 | 0.553 |
LIG_SUMO_SIM_par_1 | 247 | 254 | PF11976 | 0.543 |
LIG_TRAF2_1 | 336 | 339 | PF00917 | 0.441 |
LIG_TRAF2_1 | 457 | 460 | PF00917 | 0.541 |
LIG_TYR_ITIM | 448 | 453 | PF00017 | 0.578 |
MOD_CK1_1 | 119 | 125 | PF00069 | 0.732 |
MOD_CK1_1 | 234 | 240 | PF00069 | 0.706 |
MOD_CK1_1 | 51 | 57 | PF00069 | 0.574 |
MOD_CK2_1 | 142 | 148 | PF00069 | 0.609 |
MOD_Cter_Amidation | 95 | 98 | PF01082 | 0.542 |
MOD_GlcNHglycan | 191 | 194 | PF01048 | 0.642 |
MOD_GlcNHglycan | 233 | 236 | PF01048 | 0.666 |
MOD_GSK3_1 | 100 | 107 | PF00069 | 0.548 |
MOD_GSK3_1 | 124 | 131 | PF00069 | 0.704 |
MOD_GSK3_1 | 143 | 150 | PF00069 | 0.543 |
MOD_GSK3_1 | 173 | 180 | PF00069 | 0.676 |
MOD_NEK2_1 | 147 | 152 | PF00069 | 0.686 |
MOD_NEK2_1 | 437 | 442 | PF00069 | 0.552 |
MOD_NEK2_2 | 179 | 184 | PF00069 | 0.579 |
MOD_PIKK_1 | 33 | 39 | PF00454 | 0.440 |
MOD_PKA_1 | 116 | 122 | PF00069 | 0.759 |
MOD_PKA_2 | 116 | 122 | PF00069 | 0.759 |
MOD_PKA_2 | 265 | 271 | PF00069 | 0.461 |
MOD_PKA_2 | 27 | 33 | PF00069 | 0.526 |
MOD_PKA_2 | 275 | 281 | PF00069 | 0.473 |
MOD_PKA_2 | 315 | 321 | PF00069 | 0.500 |
MOD_PKA_2 | 360 | 366 | PF00069 | 0.571 |
MOD_PKA_2 | 437 | 443 | PF00069 | 0.552 |
MOD_PKA_2 | 62 | 68 | PF00069 | 0.557 |
MOD_PKB_1 | 98 | 106 | PF00069 | 0.640 |
MOD_Plk_1 | 142 | 148 | PF00069 | 0.676 |
MOD_Plk_1 | 305 | 311 | PF00069 | 0.508 |
MOD_Plk_1 | 51 | 57 | PF00069 | 0.538 |
MOD_Plk_1 | 69 | 75 | PF00069 | 0.330 |
MOD_Plk_1 | 7 | 13 | PF00069 | 0.505 |
MOD_Plk_2-3 | 143 | 149 | PF00069 | 0.601 |
MOD_Plk_2-3 | 455 | 461 | PF00069 | 0.607 |
MOD_ProDKin_1 | 166 | 172 | PF00069 | 0.693 |
MOD_ProDKin_1 | 173 | 179 | PF00069 | 0.690 |
MOD_ProDKin_1 | 196 | 202 | PF00069 | 0.750 |
MOD_ProDKin_1 | 226 | 232 | PF00069 | 0.656 |
MOD_SUMO_for_1 | 32 | 35 | PF00179 | 0.523 |
MOD_SUMO_for_1 | 409 | 412 | PF00179 | 0.479 |
MOD_SUMO_rev_2 | 289 | 295 | PF00179 | 0.414 |
MOD_SUMO_rev_2 | 420 | 430 | PF00179 | 0.621 |
TRG_DiLeu_BaEn_1 | 213 | 218 | PF01217 | 0.583 |
TRG_DiLeu_BaEn_4 | 253 | 259 | PF01217 | 0.419 |
TRG_DiLeu_BaEn_4 | 420 | 426 | PF01217 | 0.436 |
TRG_DiLeu_BaLyEn_6 | 63 | 68 | PF01217 | 0.433 |
TRG_ENDOCYTIC_2 | 29 | 32 | PF00928 | 0.486 |
TRG_ENDOCYTIC_2 | 367 | 370 | PF00928 | 0.538 |
TRG_ENDOCYTIC_2 | 450 | 453 | PF00928 | 0.535 |
TRG_ER_diArg_1 | 116 | 118 | PF00400 | 0.753 |
TRG_ER_diArg_1 | 194 | 196 | PF00400 | 0.594 |
TRG_ER_diArg_1 | 348 | 350 | PF00400 | 0.468 |
TRG_ER_diArg_1 | 416 | 418 | PF00400 | 0.459 |
TRG_ER_diArg_1 | 446 | 448 | PF00400 | 0.575 |
TRG_ER_diArg_1 | 95 | 98 | PF00400 | 0.465 |
TRG_NES_CRM1_1 | 331 | 347 | PF08389 | 0.447 |
TRG_NES_CRM1_1 | 426 | 439 | PF08389 | 0.456 |
TRG_Pf-PMV_PEXEL_1 | 100 | 105 | PF00026 | 0.515 |
TRG_Pf-PMV_PEXEL_1 | 286 | 291 | PF00026 | 0.442 |
TRG_Pf-PMV_PEXEL_1 | 310 | 314 | PF00026 | 0.564 |
TRG_Pf-PMV_PEXEL_1 | 417 | 421 | PF00026 | 0.467 |
TRG_Pf-PMV_PEXEL_1 | 66 | 70 | PF00026 | 0.461 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P310 | Leptomonas seymouri | 53% | 85% |
A0A0S4IYQ0 | Bodo saltans | 26% | 100% |
A0A1X0NVG8 | Trypanosomatidae | 31% | 100% |
A0A3Q8IB95 | Leishmania donovani | 95% | 100% |
A0A3R7L4W3 | Trypanosoma rangeli | 34% | 100% |
A4H6J6 | Leishmania braziliensis | 81% | 85% |
A4HUY1 | Leishmania infantum | 96% | 85% |
E9ANL6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
V5C199 | Trypanosoma cruzi | 34% | 100% |