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 | 11 |
GO:0012506 | vesicle membrane | 4 | 2 |
GO:0016020 | membrane | 2 | 11 |
GO:0020018 | ciliary pocket membrane | 6 | 2 |
GO:0030659 | cytoplasmic vesicle membrane | 5 | 2 |
GO:0030662 | coated vesicle membrane | 5 | 2 |
GO:0030665 | clathrin-coated vesicle membrane | 6 | 2 |
GO:0031090 | organelle membrane | 3 | 11 |
GO:0031253 | cell projection membrane | 4 | 11 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0034464 | BBSome | 2 | 2 |
GO:0035869 | ciliary transition zone | 2 | 2 |
GO:0036064 | ciliary basal body | 3 | 2 |
GO:0060170 | ciliary membrane | 5 | 11 |
GO:0098588 | bounding membrane of organelle | 4 | 11 |
GO:0098590 | plasma membrane region | 3 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
Related structures:
AlphaFold database: Q4Q1J3
Term | Name | Level | Count |
---|---|---|---|
GO:0000041 | transition metal ion transport | 7 | 2 |
GO:0006810 | transport | 3 | 2 |
GO:0006811 | monoatomic ion transport | 4 | 2 |
GO:0006812 | monoatomic cation transport | 5 | 2 |
GO:0006826 | iron ion transport | 8 | 2 |
GO:0006996 | organelle organization | 4 | 2 |
GO:0008104 | protein localization | 4 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0015031 | protein transport | 4 | 2 |
GO:0016043 | cellular component organization | 3 | 2 |
GO:0022607 | cellular component assembly | 4 | 2 |
GO:0030001 | metal ion transport | 6 | 2 |
GO:0030030 | cell projection organization | 4 | 2 |
GO:0030031 | cell projection assembly | 5 | 2 |
GO:0033036 | macromolecule localization | 2 | 2 |
GO:0033365 | protein localization to organelle | 5 | 2 |
GO:0033572 | transferrin transport | 5 | 2 |
GO:0044782 | cilium organization | 5 | 2 |
GO:0045184 | establishment of protein localization | 3 | 2 |
GO:0051179 | localization | 1 | 2 |
GO:0051234 | establishment of localization | 2 | 2 |
GO:0051641 | cellular localization | 2 | 2 |
GO:0060271 | cilium assembly | 6 | 2 |
GO:0061512 | protein localization to cilium | 6 | 2 |
GO:0070727 | cellular macromolecule localization | 3 | 2 |
GO:0070925 | organelle assembly | 5 | 2 |
GO:0071702 | organic substance transport | 4 | 2 |
GO:0071705 | nitrogen compound transport | 4 | 2 |
GO:0071840 | cellular component organization or biogenesis | 2 | 2 |
GO:0120031 | plasma membrane bounded cell projection assembly | 6 | 2 |
GO:0120036 | plasma membrane bounded cell projection organization | 5 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 2 |
GO:0005515 | protein binding | 2 | 2 |
GO:0030276 | clathrin binding | 3 | 2 |
GO:0032050 | clathrin heavy chain binding | 4 | 2 |
GO:0032182 | ubiquitin-like protein binding | 3 | 2 |
GO:0043130 | ubiquitin binding | 4 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 269 | 273 | PF00656 | 0.424 |
CLV_C14_Caspase3-7 | 471 | 475 | PF00656 | 0.487 |
CLV_NRD_NRD_1 | 183 | 185 | PF00675 | 0.532 |
CLV_NRD_NRD_1 | 187 | 189 | PF00675 | 0.431 |
CLV_NRD_NRD_1 | 328 | 330 | PF00675 | 0.307 |
CLV_NRD_NRD_1 | 444 | 446 | PF00675 | 0.471 |
CLV_NRD_NRD_1 | 6 | 8 | PF00675 | 0.687 |
CLV_NRD_NRD_1 | 64 | 66 | PF00675 | 0.328 |
CLV_PCSK_FUR_1 | 62 | 66 | PF00082 | 0.346 |
CLV_PCSK_KEX2_1 | 107 | 109 | PF00082 | 0.360 |
CLV_PCSK_KEX2_1 | 183 | 185 | PF00082 | 0.361 |
CLV_PCSK_KEX2_1 | 187 | 189 | PF00082 | 0.327 |
CLV_PCSK_KEX2_1 | 444 | 446 | PF00082 | 0.471 |
CLV_PCSK_KEX2_1 | 64 | 66 | PF00082 | 0.328 |
CLV_PCSK_PC1ET2_1 | 107 | 109 | PF00082 | 0.340 |
CLV_PCSK_PC7_1 | 183 | 189 | PF00082 | 0.319 |
CLV_PCSK_SKI1_1 | 103 | 107 | PF00082 | 0.276 |
CLV_PCSK_SKI1_1 | 161 | 165 | PF00082 | 0.460 |
CLV_PCSK_SKI1_1 | 211 | 215 | PF00082 | 0.393 |
CLV_PCSK_SKI1_1 | 262 | 266 | PF00082 | 0.313 |
CLV_PCSK_SKI1_1 | 318 | 322 | PF00082 | 0.361 |
CLV_PCSK_SKI1_1 | 330 | 334 | PF00082 | 0.460 |
DEG_APCC_DBOX_1 | 64 | 72 | PF00400 | 0.446 |
DEG_MDM2_SWIB_1 | 432 | 439 | PF02201 | 0.469 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.675 |
DEG_SPOP_SBC_1 | 469 | 473 | PF00917 | 0.692 |
DOC_CKS1_1 | 438 | 443 | PF01111 | 0.438 |
DOC_CYCLIN_RxL_1 | 100 | 110 | PF00134 | 0.302 |
DOC_MAPK_gen_1 | 62 | 71 | PF00069 | 0.463 |
DOC_PP2B_LxvP_1 | 462 | 465 | PF13499 | 0.487 |
DOC_PP4_FxxP_1 | 333 | 336 | PF00568 | 0.444 |
DOC_USP7_MATH_1 | 276 | 280 | PF00917 | 0.286 |
DOC_USP7_MATH_1 | 477 | 481 | PF00917 | 0.693 |
DOC_USP7_UBL2_3 | 103 | 107 | PF12436 | 0.312 |
DOC_WW_Pin1_4 | 124 | 129 | PF00397 | 0.420 |
DOC_WW_Pin1_4 | 230 | 235 | PF00397 | 0.238 |
DOC_WW_Pin1_4 | 264 | 269 | PF00397 | 0.248 |
DOC_WW_Pin1_4 | 31 | 36 | PF00397 | 0.595 |
DOC_WW_Pin1_4 | 437 | 442 | PF00397 | 0.490 |
LIG_14-3-3_CanoR_1 | 329 | 333 | PF00244 | 0.355 |
LIG_14-3-3_CanoR_1 | 354 | 362 | PF00244 | 0.406 |
LIG_Actin_WH2_2 | 313 | 331 | PF00022 | 0.333 |
LIG_APCC_ABBA_1 | 223 | 228 | PF00400 | 0.279 |
LIG_APCC_ABBA_1 | 366 | 371 | PF00400 | 0.325 |
LIG_BIR_III_2 | 474 | 478 | PF00653 | 0.484 |
LIG_FHA_1 | 120 | 126 | PF00498 | 0.372 |
LIG_FHA_2 | 233 | 239 | PF00498 | 0.361 |
LIG_FHA_2 | 267 | 273 | PF00498 | 0.428 |
LIG_IRF3_LxIS_1 | 260 | 267 | PF10401 | 0.226 |
LIG_LIR_Apic_2 | 331 | 336 | PF02991 | 0.426 |
LIG_LIR_Gen_1 | 203 | 214 | PF02991 | 0.433 |
LIG_LIR_Gen_1 | 321 | 328 | PF02991 | 0.344 |
LIG_LIR_Gen_1 | 424 | 432 | PF02991 | 0.356 |
LIG_LIR_Nem_3 | 173 | 178 | PF02991 | 0.462 |
LIG_LIR_Nem_3 | 203 | 209 | PF02991 | 0.435 |
LIG_LIR_Nem_3 | 292 | 297 | PF02991 | 0.371 |
LIG_LIR_Nem_3 | 321 | 325 | PF02991 | 0.380 |
LIG_LIR_Nem_3 | 404 | 409 | PF02991 | 0.427 |
LIG_LIR_Nem_3 | 424 | 429 | PF02991 | 0.393 |
LIG_LIR_Nem_3 | 95 | 101 | PF02991 | 0.303 |
LIG_NRBOX | 457 | 463 | PF00104 | 0.407 |
LIG_NRBOX | 67 | 73 | PF00104 | 0.352 |
LIG_PCNA_TLS_4 | 187 | 194 | PF02747 | 0.310 |
LIG_Pex14_1 | 170 | 174 | PF04695 | 0.307 |
LIG_Pex14_1 | 339 | 343 | PF04695 | 0.274 |
LIG_Pex14_2 | 333 | 337 | PF04695 | 0.415 |
LIG_Pex14_2 | 432 | 436 | PF04695 | 0.339 |
LIG_SH2_CRK | 294 | 298 | PF00017 | 0.371 |
LIG_SH2_CRK | 322 | 326 | PF00017 | 0.425 |
LIG_SH2_GRB2like | 409 | 412 | PF00017 | 0.405 |
LIG_SH2_GRB2like | 78 | 81 | PF00017 | 0.353 |
LIG_SH2_NCK_1 | 322 | 326 | PF00017 | 0.449 |
LIG_SH2_PTP2 | 175 | 178 | PF00017 | 0.415 |
LIG_SH2_SRC | 226 | 229 | PF00017 | 0.371 |
LIG_SH2_SRC | 396 | 399 | PF00017 | 0.430 |
LIG_SH2_STAP1 | 219 | 223 | PF00017 | 0.279 |
LIG_SH2_STAP1 | 226 | 230 | PF00017 | 0.279 |
LIG_SH2_STAP1 | 287 | 291 | PF00017 | 0.371 |
LIG_SH2_STAP1 | 322 | 326 | PF00017 | 0.466 |
LIG_SH2_STAP1 | 396 | 400 | PF00017 | 0.334 |
LIG_SH2_STAP1 | 412 | 416 | PF00017 | 0.158 |
LIG_SH2_STAP1 | 78 | 82 | PF00017 | 0.309 |
LIG_SH2_STAP1 | 98 | 102 | PF00017 | 0.175 |
LIG_SH2_STAT3 | 247 | 250 | PF00017 | 0.286 |
LIG_SH2_STAT3 | 73 | 76 | PF00017 | 0.323 |
LIG_SH2_STAT5 | 101 | 104 | PF00017 | 0.293 |
LIG_SH2_STAT5 | 175 | 178 | PF00017 | 0.336 |
LIG_SH2_STAT5 | 206 | 209 | PF00017 | 0.427 |
LIG_SH2_STAT5 | 247 | 250 | PF00017 | 0.266 |
LIG_SH2_STAT5 | 259 | 262 | PF00017 | 0.253 |
LIG_SH2_STAT5 | 355 | 358 | PF00017 | 0.319 |
LIG_SH2_STAT5 | 409 | 412 | PF00017 | 0.334 |
LIG_SH2_STAT5 | 73 | 76 | PF00017 | 0.323 |
LIG_SH3_3 | 231 | 237 | PF00018 | 0.322 |
LIG_SH3_3 | 29 | 35 | PF00018 | 0.562 |
LIG_SH3_3 | 462 | 468 | PF00018 | 0.630 |
LIG_SUMO_SIM_anti_2 | 114 | 122 | PF11976 | 0.437 |
LIG_TRAF2_1 | 153 | 156 | PF00917 | 0.407 |
LIG_TRAF2_1 | 421 | 424 | PF00917 | 0.349 |
MOD_CDC14_SPxK_1 | 34 | 37 | PF00782 | 0.527 |
MOD_CDK_SPxK_1 | 31 | 37 | PF00069 | 0.536 |
MOD_CDK_SPxxK_3 | 437 | 444 | PF00069 | 0.484 |
MOD_CK1_1 | 39 | 45 | PF00069 | 0.553 |
MOD_CK2_1 | 109 | 115 | PF00069 | 0.369 |
MOD_CK2_1 | 418 | 424 | PF00069 | 0.390 |
MOD_Cter_Amidation | 316 | 319 | PF01082 | 0.438 |
MOD_Cter_Amidation | 5 | 8 | PF01082 | 0.742 |
MOD_GlcNHglycan | 283 | 286 | PF01048 | 0.356 |
MOD_GlcNHglycan | 303 | 306 | PF01048 | 0.151 |
MOD_GlcNHglycan | 356 | 359 | PF01048 | 0.300 |
MOD_GlcNHglycan | 38 | 42 | PF01048 | 0.501 |
MOD_GlcNHglycan | 478 | 482 | PF01048 | 0.715 |
MOD_GSK3_1 | 109 | 116 | PF00069 | 0.364 |
MOD_GSK3_1 | 12 | 19 | PF00069 | 0.558 |
MOD_GSK3_1 | 228 | 235 | PF00069 | 0.379 |
MOD_GSK3_1 | 262 | 269 | PF00069 | 0.320 |
MOD_GSK3_1 | 39 | 46 | PF00069 | 0.546 |
MOD_N-GLC_2 | 391 | 393 | PF02516 | 0.332 |
MOD_NEK2_1 | 109 | 114 | PF00069 | 0.254 |
MOD_NEK2_1 | 119 | 124 | PF00069 | 0.267 |
MOD_NEK2_1 | 17 | 22 | PF00069 | 0.706 |
MOD_NEK2_1 | 193 | 198 | PF00069 | 0.356 |
MOD_NEK2_1 | 28 | 33 | PF00069 | 0.636 |
MOD_NEK2_1 | 328 | 333 | PF00069 | 0.419 |
MOD_NEK2_1 | 89 | 94 | PF00069 | 0.457 |
MOD_NEK2_2 | 412 | 417 | PF00069 | 0.322 |
MOD_PIKK_1 | 132 | 138 | PF00454 | 0.379 |
MOD_PK_1 | 418 | 424 | PF00069 | 0.330 |
MOD_PKA_1 | 318 | 324 | PF00069 | 0.349 |
MOD_PKA_2 | 328 | 334 | PF00069 | 0.412 |
MOD_PKA_2 | 36 | 42 | PF00069 | 0.676 |
MOD_PKA_2 | 89 | 95 | PF00069 | 0.484 |
MOD_Plk_1 | 445 | 451 | PF00069 | 0.540 |
MOD_Plk_4 | 276 | 282 | PF00069 | 0.286 |
MOD_Plk_4 | 328 | 334 | PF00069 | 0.419 |
MOD_Plk_4 | 412 | 418 | PF00069 | 0.417 |
MOD_Plk_4 | 446 | 452 | PF00069 | 0.520 |
MOD_ProDKin_1 | 124 | 130 | PF00069 | 0.419 |
MOD_ProDKin_1 | 230 | 236 | PF00069 | 0.238 |
MOD_ProDKin_1 | 264 | 270 | PF00069 | 0.242 |
MOD_ProDKin_1 | 31 | 37 | PF00069 | 0.595 |
MOD_ProDKin_1 | 437 | 443 | PF00069 | 0.491 |
TRG_DiLeu_BaEn_1 | 115 | 120 | PF01217 | 0.425 |
TRG_DiLeu_BaEn_1 | 446 | 451 | PF01217 | 0.458 |
TRG_ENDOCYTIC_2 | 175 | 178 | PF00928 | 0.320 |
TRG_ENDOCYTIC_2 | 206 | 209 | PF00928 | 0.410 |
TRG_ENDOCYTIC_2 | 294 | 297 | PF00928 | 0.371 |
TRG_ENDOCYTIC_2 | 322 | 325 | PF00928 | 0.443 |
TRG_ENDOCYTIC_2 | 426 | 429 | PF00928 | 0.368 |
TRG_ER_diArg_1 | 186 | 188 | PF00400 | 0.451 |
TRG_NES_CRM1_1 | 115 | 129 | PF08389 | 0.447 |
TRG_NES_CRM1_1 | 238 | 250 | PF08389 | 0.255 |
TRG_Pf-PMV_PEXEL_1 | 456 | 460 | PF00026 | 0.480 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PED7 | Leptomonas seymouri | 70% | 100% |
A0A1X0P7L4 | Trypanosomatidae | 47% | 87% |
A0A3Q8IH89 | Leishmania donovani | 98% | 100% |
A0A3R7MGH4 | Trypanosoma rangeli | 48% | 100% |
A1Z8E9 | Drosophila melanogaster | 31% | 100% |
A4HP97 | Leishmania braziliensis | 84% | 100% |
A4IDK2 | Leishmania infantum | 98% | 100% |
D0A3A0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 49% | 100% |
E9AT05 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
Q1JQ97 | Bos taurus | 42% | 95% |
Q28G25 | Xenopus tropicalis | 42% | 96% |
Q5CZ52 | Caenorhabditis elegans | 27% | 100% |
Q8C1Z7 | Mus musculus | 43% | 95% |
Q96RK4 | Homo sapiens | 44% | 95% |
Q9STS3 | Arabidopsis thaliana | 20% | 85% |
V5BSG3 | Trypanosoma cruzi | 20% | 70% |
V5DCK5 | Trypanosoma cruzi | 47% | 100% |