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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005930 | axoneme | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A0A3Q8IHP2
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 12 |
GO:0005509 | calcium ion binding | 5 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043169 | cation binding | 3 | 12 |
GO:0046872 | metal ion binding | 4 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 163 | 167 | PF00656 | 0.460 |
CLV_C14_Caspase3-7 | 309 | 313 | PF00656 | 0.328 |
CLV_C14_Caspase3-7 | 345 | 349 | PF00656 | 0.474 |
CLV_NRD_NRD_1 | 104 | 106 | PF00675 | 0.412 |
CLV_NRD_NRD_1 | 151 | 153 | PF00675 | 0.555 |
CLV_NRD_NRD_1 | 359 | 361 | PF00675 | 0.597 |
CLV_PCSK_KEX2_1 | 104 | 106 | PF00082 | 0.338 |
CLV_PCSK_KEX2_1 | 19 | 21 | PF00082 | 0.425 |
CLV_PCSK_PC1ET2_1 | 19 | 21 | PF00082 | 0.508 |
CLV_PCSK_SKI1_1 | 19 | 23 | PF00082 | 0.406 |
CLV_PCSK_SKI1_1 | 242 | 246 | PF00082 | 0.492 |
CLV_PCSK_SKI1_1 | 332 | 336 | PF00082 | 0.426 |
CLV_PCSK_SKI1_1 | 370 | 374 | PF00082 | 0.462 |
DEG_APCC_DBOX_1 | 104 | 112 | PF00400 | 0.328 |
DEG_APCC_DBOX_1 | 241 | 249 | PF00400 | 0.505 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.697 |
DOC_CYCLIN_RxL_1 | 16 | 26 | PF00134 | 0.430 |
DOC_CYCLIN_RxL_1 | 262 | 270 | PF00134 | 0.436 |
DOC_PP2B_LxvP_1 | 296 | 299 | PF13499 | 0.504 |
DOC_PP2B_LxvP_1 | 323 | 326 | PF13499 | 0.456 |
DOC_USP7_MATH_1 | 179 | 183 | PF00917 | 0.480 |
DOC_USP7_MATH_1 | 202 | 206 | PF00917 | 0.504 |
DOC_USP7_MATH_1 | 234 | 238 | PF00917 | 0.578 |
DOC_USP7_MATH_1 | 240 | 244 | PF00917 | 0.494 |
DOC_USP7_MATH_1 | 299 | 303 | PF00917 | 0.577 |
DOC_WW_Pin1_4 | 23 | 28 | PF00397 | 0.624 |
DOC_WW_Pin1_4 | 363 | 368 | PF00397 | 0.590 |
DOC_WW_Pin1_4 | 98 | 103 | PF00397 | 0.390 |
LIG_Actin_WH2_2 | 88 | 106 | PF00022 | 0.490 |
LIG_BRCT_BRCA1_1 | 204 | 208 | PF00533 | 0.532 |
LIG_BRCT_BRCA1_1 | 340 | 344 | PF00533 | 0.514 |
LIG_eIF4E_1 | 319 | 325 | PF01652 | 0.481 |
LIG_FHA_1 | 291 | 297 | PF00498 | 0.478 |
LIG_FHA_1 | 299 | 305 | PF00498 | 0.238 |
LIG_FHA_1 | 88 | 94 | PF00498 | 0.368 |
LIG_FHA_2 | 145 | 151 | PF00498 | 0.558 |
LIG_FHA_2 | 161 | 167 | PF00498 | 0.457 |
LIG_FHA_2 | 307 | 313 | PF00498 | 0.340 |
LIG_FHA_2 | 373 | 379 | PF00498 | 0.478 |
LIG_FHA_2 | 50 | 56 | PF00498 | 0.354 |
LIG_FHA_2 | 75 | 81 | PF00498 | 0.449 |
LIG_LIR_Apic_2 | 348 | 354 | PF02991 | 0.512 |
LIG_LIR_Gen_1 | 188 | 198 | PF02991 | 0.396 |
LIG_LIR_Gen_1 | 406 | 413 | PF02991 | 0.440 |
LIG_LIR_Gen_1 | 90 | 100 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 173 | 177 | PF02991 | 0.378 |
LIG_LIR_Nem_3 | 188 | 194 | PF02991 | 0.326 |
LIG_LIR_Nem_3 | 406 | 412 | PF02991 | 0.474 |
LIG_LIR_Nem_3 | 90 | 95 | PF02991 | 0.447 |
LIG_Pex14_1 | 340 | 344 | PF04695 | 0.487 |
LIG_Pex14_2 | 155 | 159 | PF04695 | 0.432 |
LIG_Pex14_2 | 373 | 377 | PF04695 | 0.393 |
LIG_RPA_C_Fungi | 233 | 245 | PF08784 | 0.544 |
LIG_SH2_CRK | 178 | 182 | PF00017 | 0.386 |
LIG_SH2_CRK | 351 | 355 | PF00017 | 0.503 |
LIG_SH2_STAP1 | 320 | 324 | PF00017 | 0.479 |
LIG_SH2_STAT3 | 396 | 399 | PF00017 | 0.466 |
LIG_SH2_STAT5 | 297 | 300 | PF00017 | 0.417 |
LIG_SH2_STAT5 | 396 | 399 | PF00017 | 0.413 |
LIG_SUMO_SIM_anti_2 | 188 | 196 | PF11976 | 0.371 |
LIG_SUMO_SIM_anti_2 | 90 | 97 | PF11976 | 0.475 |
LIG_TRAF2_1 | 170 | 173 | PF00917 | 0.403 |
LIG_TRAF2_1 | 52 | 55 | PF00917 | 0.448 |
LIG_TRAF2_1 | 59 | 62 | PF00917 | 0.402 |
LIG_TRAF2_1 | 66 | 69 | PF00917 | 0.377 |
LIG_UBA3_1 | 75 | 84 | PF00899 | 0.473 |
LIG_WRC_WIRS_1 | 33 | 38 | PF05994 | 0.549 |
MOD_CDC14_SPxK_1 | 101 | 104 | PF00782 | 0.477 |
MOD_CDK_SPxK_1 | 98 | 104 | PF00069 | 0.384 |
MOD_CDK_SPxxK_3 | 363 | 370 | PF00069 | 0.585 |
MOD_CDK_SPxxK_3 | 98 | 105 | PF00069 | 0.425 |
MOD_CK1_1 | 222 | 228 | PF00069 | 0.607 |
MOD_CK2_1 | 144 | 150 | PF00069 | 0.545 |
MOD_CK2_1 | 167 | 173 | PF00069 | 0.411 |
MOD_CK2_1 | 225 | 231 | PF00069 | 0.573 |
MOD_CK2_1 | 299 | 305 | PF00069 | 0.538 |
MOD_CK2_1 | 339 | 345 | PF00069 | 0.501 |
MOD_CK2_1 | 49 | 55 | PF00069 | 0.404 |
MOD_CK2_1 | 63 | 69 | PF00069 | 0.267 |
MOD_GlcNHglycan | 156 | 159 | PF01048 | 0.521 |
MOD_GlcNHglycan | 169 | 172 | PF01048 | 0.545 |
MOD_GlcNHglycan | 181 | 184 | PF01048 | 0.412 |
MOD_GlcNHglycan | 242 | 245 | PF01048 | 0.559 |
MOD_GlcNHglycan | 259 | 262 | PF01048 | 0.476 |
MOD_GlcNHglycan | 27 | 30 | PF01048 | 0.470 |
MOD_GlcNHglycan | 278 | 281 | PF01048 | 0.467 |
MOD_GlcNHglycan | 328 | 331 | PF01048 | 0.528 |
MOD_GlcNHglycan | 399 | 402 | PF01048 | 0.476 |
MOD_GSK3_1 | 202 | 209 | PF00069 | 0.480 |
MOD_GSK3_1 | 230 | 237 | PF00069 | 0.488 |
MOD_GSK3_1 | 240 | 247 | PF00069 | 0.468 |
MOD_GSK3_1 | 276 | 283 | PF00069 | 0.473 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.476 |
MOD_GSK3_1 | 45 | 52 | PF00069 | 0.449 |
MOD_GSK3_1 | 83 | 90 | PF00069 | 0.444 |
MOD_N-GLC_1 | 159 | 164 | PF02516 | 0.489 |
MOD_N-GLC_1 | 299 | 304 | PF02516 | 0.486 |
MOD_N-GLC_1 | 98 | 103 | PF02516 | 0.499 |
MOD_NEK2_1 | 11 | 16 | PF00069 | 0.480 |
MOD_NEK2_1 | 159 | 164 | PF00069 | 0.480 |
MOD_NEK2_1 | 208 | 213 | PF00069 | 0.472 |
MOD_NEK2_1 | 267 | 272 | PF00069 | 0.454 |
MOD_NEK2_1 | 339 | 344 | PF00069 | 0.377 |
MOD_NEK2_1 | 36 | 41 | PF00069 | 0.522 |
MOD_NEK2_1 | 46 | 51 | PF00069 | 0.480 |
MOD_PIKK_1 | 46 | 52 | PF00454 | 0.600 |
MOD_PK_1 | 206 | 212 | PF00069 | 0.396 |
MOD_Plk_1 | 187 | 193 | PF00069 | 0.391 |
MOD_Plk_1 | 206 | 212 | PF00069 | 0.504 |
MOD_Plk_1 | 225 | 231 | PF00069 | 0.536 |
MOD_Plk_1 | 299 | 305 | PF00069 | 0.514 |
MOD_Plk_4 | 187 | 193 | PF00069 | 0.377 |
MOD_Plk_4 | 244 | 250 | PF00069 | 0.455 |
MOD_Plk_4 | 299 | 305 | PF00069 | 0.482 |
MOD_ProDKin_1 | 23 | 29 | PF00069 | 0.623 |
MOD_ProDKin_1 | 363 | 369 | PF00069 | 0.585 |
MOD_ProDKin_1 | 98 | 104 | PF00069 | 0.384 |
MOD_SUMO_for_1 | 213 | 216 | PF00179 | 0.516 |
MOD_SUMO_rev_2 | 161 | 170 | PF00179 | 0.567 |
TRG_DiLeu_BaEn_1 | 388 | 393 | PF01217 | 0.449 |
TRG_DiLeu_BaLyEn_6 | 17 | 22 | PF01217 | 0.408 |
TRG_ENDOCYTIC_2 | 178 | 181 | PF00928 | 0.386 |
TRG_ENDOCYTIC_2 | 320 | 323 | PF00928 | 0.359 |
TRG_ER_diArg_1 | 103 | 105 | PF00400 | 0.382 |
TRG_Pf-PMV_PEXEL_1 | 20 | 24 | PF00026 | 0.502 |
TRG_Pf-PMV_PEXEL_1 | 58 | 62 | PF00026 | 0.467 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I2R2 | Leptomonas seymouri | 66% | 100% |
A0A0S4J207 | Bodo saltans | 35% | 97% |
A0A1X0PAP2 | Trypanosomatidae | 42% | 100% |
A0A422N4H8 | Trypanosoma rangeli | 42% | 100% |
A4HB14 | Leishmania braziliensis | 84% | 100% |
A4IA71 | Leishmania infantum | 99% | 100% |
C9ZM35 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 100% |
E9B584 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
Q4Q2P9 | Leishmania major | 95% | 100% |
V5B5A3 | Trypanosoma cruzi | 42% | 100% |