Flagella, MORN repeat
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:0005829 | cytosol | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pescher et al. (upgregulation) | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Lahav et al. - mRNA
- Protein
|
Related structures:
AlphaFold database: A4HYQ3
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 181 | 185 | PF00656 | 0.270 |
CLV_C14_Caspase3-7 | 319 | 323 | PF00656 | 0.442 |
CLV_C14_Caspase3-7 | 376 | 380 | PF00656 | 0.527 |
CLV_C14_Caspase3-7 | 64 | 68 | PF00656 | 0.539 |
CLV_NRD_NRD_1 | 328 | 330 | PF00675 | 0.549 |
CLV_PCSK_KEX2_1 | 209 | 211 | PF00082 | 0.345 |
CLV_PCSK_KEX2_1 | 328 | 330 | PF00082 | 0.549 |
CLV_PCSK_PC1ET2_1 | 209 | 211 | PF00082 | 0.345 |
CLV_PCSK_SKI1_1 | 305 | 309 | PF00082 | 0.403 |
CLV_PCSK_SKI1_1 | 373 | 377 | PF00082 | 0.488 |
DEG_COP1_1 | 2 | 9 | PF00400 | 0.577 |
DEG_SPOP_SBC_1 | 119 | 123 | PF00917 | 0.586 |
DEG_SPOP_SBC_1 | 16 | 20 | PF00917 | 0.517 |
DEG_SPOP_SBC_1 | 394 | 398 | PF00917 | 0.546 |
DOC_ANK_TNKS_1 | 387 | 394 | PF00023 | 0.489 |
DOC_MAPK_gen_1 | 209 | 219 | PF00069 | 0.246 |
DOC_MAPK_gen_1 | 278 | 287 | PF00069 | 0.242 |
DOC_MAPK_MEF2A_6 | 210 | 219 | PF00069 | 0.246 |
DOC_PP1_RVXF_1 | 142 | 149 | PF00149 | 0.374 |
DOC_PP2B_LxvP_1 | 285 | 288 | PF13499 | 0.335 |
DOC_PP2B_LxvP_1 | 335 | 338 | PF13499 | 0.486 |
DOC_USP7_MATH_1 | 118 | 122 | PF00917 | 0.607 |
DOC_USP7_MATH_1 | 394 | 398 | PF00917 | 0.610 |
DOC_USP7_MATH_1 | 40 | 44 | PF00917 | 0.584 |
DOC_USP7_MATH_1 | 89 | 93 | PF00917 | 0.571 |
DOC_USP7_MATH_1 | 96 | 100 | PF00917 | 0.506 |
DOC_WW_Pin1_4 | 113 | 118 | PF00397 | 0.550 |
DOC_WW_Pin1_4 | 30 | 35 | PF00397 | 0.589 |
DOC_WW_Pin1_4 | 305 | 310 | PF00397 | 0.344 |
LIG_Actin_WH2_2 | 150 | 166 | PF00022 | 0.346 |
LIG_BH_BH3_1 | 54 | 70 | PF00452 | 0.401 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.576 |
LIG_BIR_III_4 | 322 | 326 | PF00653 | 0.472 |
LIG_DLG_GKlike_1 | 363 | 371 | PF00625 | 0.406 |
LIG_FHA_1 | 141 | 147 | PF00498 | 0.334 |
LIG_FHA_1 | 348 | 354 | PF00498 | 0.398 |
LIG_FHA_1 | 45 | 51 | PF00498 | 0.528 |
LIG_FHA_1 | 89 | 95 | PF00498 | 0.559 |
LIG_FHA_2 | 306 | 312 | PF00498 | 0.407 |
LIG_FHA_2 | 356 | 362 | PF00498 | 0.397 |
LIG_FHA_2 | 374 | 380 | PF00498 | 0.584 |
LIG_FHA_2 | 396 | 402 | PF00498 | 0.572 |
LIG_FHA_2 | 59 | 65 | PF00498 | 0.673 |
LIG_Integrin_RGD_1 | 243 | 245 | PF01839 | 0.324 |
LIG_LIR_Gen_1 | 238 | 247 | PF02991 | 0.387 |
LIG_LIR_Nem_3 | 238 | 242 | PF02991 | 0.368 |
LIG_LIR_Nem_3 | 301 | 307 | PF02991 | 0.381 |
LIG_MYND_1 | 333 | 337 | PF01753 | 0.486 |
LIG_Pex14_2 | 270 | 274 | PF04695 | 0.242 |
LIG_PTAP_UEV_1 | 329 | 334 | PF05743 | 0.484 |
LIG_REV1ctd_RIR_1 | 301 | 308 | PF16727 | 0.371 |
LIG_RPA_C_Fungi | 358 | 370 | PF08784 | 0.428 |
LIG_SH2_CRK | 239 | 243 | PF00017 | 0.370 |
LIG_SH2_STAT3 | 153 | 156 | PF00017 | 0.318 |
LIG_SH2_STAT3 | 247 | 250 | PF00017 | 0.221 |
LIG_SH2_STAT5 | 153 | 156 | PF00017 | 0.318 |
LIG_SH2_STAT5 | 178 | 181 | PF00017 | 0.242 |
LIG_SH2_STAT5 | 216 | 219 | PF00017 | 0.245 |
LIG_SH3_3 | 1 | 7 | PF00018 | 0.575 |
LIG_SH3_3 | 31 | 37 | PF00018 | 0.733 |
LIG_SH3_3 | 327 | 333 | PF00018 | 0.546 |
LIG_SH3_3 | 381 | 387 | PF00018 | 0.482 |
LIG_SH3_4 | 232 | 239 | PF00018 | 0.270 |
LIG_SUMO_SIM_par_1 | 46 | 51 | PF11976 | 0.479 |
LIG_TRAF2_1 | 420 | 423 | PF00917 | 0.502 |
LIG_WW_3 | 336 | 340 | PF00397 | 0.489 |
MOD_CDK_SPxxK_3 | 113 | 120 | PF00069 | 0.534 |
MOD_CK1_1 | 121 | 127 | PF00069 | 0.610 |
MOD_CK1_1 | 15 | 21 | PF00069 | 0.522 |
MOD_CK1_1 | 331 | 337 | PF00069 | 0.584 |
MOD_CK1_1 | 345 | 351 | PF00069 | 0.387 |
MOD_CK1_1 | 397 | 403 | PF00069 | 0.615 |
MOD_CK1_1 | 43 | 49 | PF00069 | 0.670 |
MOD_CK2_1 | 127 | 133 | PF00069 | 0.662 |
MOD_CK2_1 | 305 | 311 | PF00069 | 0.401 |
MOD_CK2_1 | 355 | 361 | PF00069 | 0.398 |
MOD_CK2_1 | 417 | 423 | PF00069 | 0.498 |
MOD_CK2_1 | 48 | 54 | PF00069 | 0.528 |
MOD_Cter_Amidation | 207 | 210 | PF01082 | 0.242 |
MOD_Cter_Amidation | 276 | 279 | PF01082 | 0.242 |
MOD_GlcNHglycan | 129 | 132 | PF01048 | 0.601 |
MOD_GlcNHglycan | 14 | 17 | PF01048 | 0.621 |
MOD_GlcNHglycan | 210 | 213 | PF01048 | 0.278 |
MOD_GlcNHglycan | 247 | 250 | PF01048 | 0.385 |
MOD_GlcNHglycan | 330 | 333 | PF01048 | 0.541 |
MOD_GlcNHglycan | 345 | 348 | PF01048 | 0.538 |
MOD_GlcNHglycan | 42 | 45 | PF01048 | 0.584 |
MOD_GlcNHglycan | 91 | 94 | PF01048 | 0.568 |
MOD_GlcNHglycan | 98 | 101 | PF01048 | 0.646 |
MOD_GSK3_1 | 118 | 125 | PF00069 | 0.579 |
MOD_GSK3_1 | 12 | 19 | PF00069 | 0.589 |
MOD_GSK3_1 | 127 | 134 | PF00069 | 0.601 |
MOD_GSK3_1 | 26 | 33 | PF00069 | 0.495 |
MOD_GSK3_1 | 343 | 350 | PF00069 | 0.451 |
MOD_GSK3_1 | 393 | 400 | PF00069 | 0.601 |
MOD_GSK3_1 | 40 | 47 | PF00069 | 0.753 |
MOD_GSK3_1 | 54 | 61 | PF00069 | 0.484 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.568 |
MOD_N-GLC_1 | 20 | 25 | PF02516 | 0.478 |
MOD_NEK2_1 | 355 | 360 | PF00069 | 0.398 |
MOD_NEK2_2 | 380 | 385 | PF00069 | 0.452 |
MOD_PIKK_1 | 84 | 90 | PF00454 | 0.561 |
MOD_PKA_1 | 328 | 334 | PF00069 | 0.545 |
MOD_PKA_2 | 12 | 18 | PF00069 | 0.469 |
MOD_PKA_2 | 245 | 251 | PF00069 | 0.334 |
MOD_PKA_2 | 260 | 266 | PF00069 | 0.194 |
MOD_PKA_2 | 328 | 334 | PF00069 | 0.712 |
MOD_Plk_1 | 20 | 26 | PF00069 | 0.533 |
MOD_Plk_1 | 380 | 386 | PF00069 | 0.453 |
MOD_Plk_2-3 | 132 | 138 | PF00069 | 0.567 |
MOD_ProDKin_1 | 113 | 119 | PF00069 | 0.554 |
MOD_ProDKin_1 | 30 | 36 | PF00069 | 0.589 |
MOD_ProDKin_1 | 305 | 311 | PF00069 | 0.344 |
MOD_SUMO_rev_2 | 136 | 146 | PF00179 | 0.445 |
MOD_SUMO_rev_2 | 225 | 233 | PF00179 | 0.270 |
MOD_SUMO_rev_2 | 49 | 58 | PF00179 | 0.575 |
TRG_DiLeu_BaEn_1 | 142 | 147 | PF01217 | 0.371 |
TRG_DiLeu_BaLyEn_6 | 68 | 73 | PF01217 | 0.491 |
TRG_ENDOCYTIC_2 | 216 | 219 | PF00928 | 0.273 |
TRG_ENDOCYTIC_2 | 224 | 227 | PF00928 | 0.219 |
TRG_ENDOCYTIC_2 | 239 | 242 | PF00928 | 0.358 |
TRG_ER_diArg_1 | 328 | 330 | PF00400 | 0.549 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDL7 | Leptomonas seymouri | 61% | 89% |
A0A3Q8IAI5 | Leishmania donovani | 100% | 100% |
E9AIB5 | Leishmania braziliensis | 63% | 100% |
E9AUK2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |
Q4QCY2 | Leishmania major | 88% | 100% |