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: 3 |
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 | 5 |
GO:0005868 | cytoplasmic dynein complex | 4 | 11 |
GO:0005875 | microtubule associated complex | 2 | 11 |
GO:0005930 | axoneme | 2 | 2 |
GO:0030286 | dynein complex | 3 | 11 |
GO:0030990 | intraciliary transport particle | 2 | 2 |
GO:0032991 | protein-containing complex | 1 | 11 |
GO:0036064 | ciliary basal body | 3 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
GO:1902494 | catalytic complex | 2 | 11 |
GO:0005737 | cytoplasm | 2 | 9 |
GO:0005929 | cilium | 4 | 9 |
GO:0042995 | cell projection | 2 | 9 |
GO:0043226 | organelle | 2 | 9 |
GO:0043227 | membrane-bounded organelle | 3 | 9 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 9 |
Related structures:
AlphaFold database: Q4Q4U9
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 11 |
GO:0007017 | microtubule-based process | 2 | 11 |
GO:0007018 | microtubule-based movement | 3 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0010970 | transport along microtubule | 4 | 11 |
GO:0030705 | cytoskeleton-dependent intracellular transport | 4 | 11 |
GO:0031503 | protein-containing complex localization | 2 | 11 |
GO:0035721 | intraciliary retrograde transport | 4 | 11 |
GO:0035735 | intraciliary transport involved in cilium assembly | 4 | 11 |
GO:0042073 | intraciliary transport | 3 | 11 |
GO:0046907 | intracellular transport | 3 | 11 |
GO:0051179 | localization | 1 | 11 |
GO:0051234 | establishment of localization | 2 | 11 |
GO:0051641 | cellular localization | 2 | 11 |
GO:0051649 | establishment of localization in cell | 3 | 11 |
GO:0099111 | microtubule-based transport | 4 | 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 2 |
GO:0005515 | protein binding | 2 | 2 |
GO:0045504 | dynein heavy chain binding | 3 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 347 | 351 | PF00656 | 0.467 |
CLV_MEL_PAP_1 | 202 | 208 | PF00089 | 0.451 |
CLV_NRD_NRD_1 | 138 | 140 | PF00675 | 0.485 |
CLV_NRD_NRD_1 | 200 | 202 | PF00675 | 0.347 |
CLV_NRD_NRD_1 | 260 | 262 | PF00675 | 0.312 |
CLV_NRD_NRD_1 | 29 | 31 | PF00675 | 0.626 |
CLV_NRD_NRD_1 | 382 | 384 | PF00675 | 0.601 |
CLV_NRD_NRD_1 | 400 | 402 | PF00675 | 0.456 |
CLV_NRD_NRD_1 | 411 | 413 | PF00675 | 0.453 |
CLV_NRD_NRD_1 | 7 | 9 | PF00675 | 0.612 |
CLV_PCSK_KEX2_1 | 124 | 126 | PF00082 | 0.642 |
CLV_PCSK_KEX2_1 | 138 | 140 | PF00082 | 0.365 |
CLV_PCSK_KEX2_1 | 200 | 202 | PF00082 | 0.309 |
CLV_PCSK_KEX2_1 | 240 | 242 | PF00082 | 0.418 |
CLV_PCSK_KEX2_1 | 260 | 262 | PF00082 | 0.252 |
CLV_PCSK_KEX2_1 | 29 | 31 | PF00082 | 0.626 |
CLV_PCSK_KEX2_1 | 382 | 384 | PF00082 | 0.508 |
CLV_PCSK_PC1ET2_1 | 124 | 126 | PF00082 | 0.683 |
CLV_PCSK_PC1ET2_1 | 240 | 242 | PF00082 | 0.418 |
CLV_PCSK_SKI1_1 | 124 | 128 | PF00082 | 0.627 |
CLV_PCSK_SKI1_1 | 223 | 227 | PF00082 | 0.449 |
CLV_PCSK_SKI1_1 | 79 | 83 | PF00082 | 0.579 |
DEG_APCC_DBOX_1 | 240 | 248 | PF00400 | 0.347 |
DOC_CKS1_1 | 166 | 171 | PF01111 | 0.314 |
DOC_MAPK_DCC_7 | 243 | 252 | PF00069 | 0.302 |
DOC_MAPK_gen_1 | 260 | 268 | PF00069 | 0.544 |
DOC_MAPK_gen_1 | 294 | 301 | PF00069 | 0.439 |
DOC_MAPK_MEF2A_6 | 243 | 252 | PF00069 | 0.300 |
DOC_MAPK_MEF2A_6 | 319 | 326 | PF00069 | 0.440 |
DOC_PP4_FxxP_1 | 304 | 307 | PF00568 | 0.375 |
DOC_PP4_FxxP_1 | 392 | 395 | PF00568 | 0.432 |
DOC_USP7_MATH_1 | 10 | 14 | PF00917 | 0.759 |
DOC_USP7_MATH_1 | 137 | 141 | PF00917 | 0.496 |
DOC_USP7_MATH_1 | 215 | 219 | PF00917 | 0.401 |
DOC_USP7_MATH_1 | 317 | 321 | PF00917 | 0.393 |
DOC_USP7_MATH_1 | 337 | 341 | PF00917 | 0.547 |
DOC_USP7_MATH_1 | 419 | 423 | PF00917 | 0.591 |
DOC_USP7_MATH_1 | 98 | 102 | PF00917 | 0.416 |
DOC_WW_Pin1_4 | 1 | 6 | PF00397 | 0.657 |
DOC_WW_Pin1_4 | 165 | 170 | PF00397 | 0.325 |
DOC_WW_Pin1_4 | 217 | 222 | PF00397 | 0.377 |
DOC_WW_Pin1_4 | 39 | 44 | PF00397 | 0.697 |
LIG_14-3-3_CanoR_1 | 109 | 115 | PF00244 | 0.521 |
LIG_14-3-3_CanoR_1 | 125 | 134 | PF00244 | 0.547 |
LIG_14-3-3_CanoR_1 | 138 | 146 | PF00244 | 0.386 |
LIG_14-3-3_CanoR_1 | 14 | 18 | PF00244 | 0.523 |
LIG_14-3-3_CanoR_1 | 205 | 213 | PF00244 | 0.473 |
LIG_AP2alpha_2 | 378 | 380 | PF02296 | 0.500 |
LIG_Clathr_ClatBox_1 | 323 | 327 | PF01394 | 0.417 |
LIG_deltaCOP1_diTrp_1 | 354 | 360 | PF00928 | 0.422 |
LIG_FHA_1 | 102 | 108 | PF00498 | 0.358 |
LIG_FHA_1 | 127 | 133 | PF00498 | 0.418 |
LIG_FHA_1 | 194 | 200 | PF00498 | 0.358 |
LIG_FHA_1 | 247 | 253 | PF00498 | 0.300 |
LIG_FHA_1 | 68 | 74 | PF00498 | 0.456 |
LIG_FHA_1 | 76 | 82 | PF00498 | 0.447 |
LIG_FHA_1 | 89 | 95 | PF00498 | 0.398 |
LIG_FHA_2 | 128 | 134 | PF00498 | 0.437 |
LIG_FHA_2 | 313 | 319 | PF00498 | 0.544 |
LIG_FHA_2 | 32 | 38 | PF00498 | 0.630 |
LIG_LIR_Apic_2 | 302 | 307 | PF02991 | 0.412 |
LIG_LIR_Apic_2 | 354 | 359 | PF02991 | 0.390 |
LIG_LIR_Apic_2 | 389 | 395 | PF02991 | 0.469 |
LIG_LIR_Gen_1 | 157 | 167 | PF02991 | 0.478 |
LIG_LIR_Gen_1 | 329 | 339 | PF02991 | 0.379 |
LIG_LIR_Gen_1 | 72 | 81 | PF02991 | 0.416 |
LIG_LIR_LC3C_4 | 90 | 95 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 157 | 162 | PF02991 | 0.464 |
LIG_LIR_Nem_3 | 292 | 298 | PF02991 | 0.471 |
LIG_LIR_Nem_3 | 329 | 334 | PF02991 | 0.333 |
LIG_LIR_Nem_3 | 72 | 77 | PF02991 | 0.409 |
LIG_Pex14_1 | 356 | 360 | PF04695 | 0.411 |
LIG_Pex14_2 | 304 | 308 | PF04695 | 0.352 |
LIG_Pex14_2 | 360 | 364 | PF04695 | 0.433 |
LIG_Rb_pABgroove_1 | 379 | 387 | PF01858 | 0.450 |
LIG_SH2_STAT5 | 111 | 114 | PF00017 | 0.469 |
LIG_SH2_STAT5 | 275 | 278 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 312 | 315 | PF00017 | 0.465 |
LIG_SH3_2 | 25 | 30 | PF14604 | 0.599 |
LIG_SH3_3 | 163 | 169 | PF00018 | 0.319 |
LIG_SH3_3 | 22 | 28 | PF00018 | 0.609 |
LIG_SH3_3 | 304 | 310 | PF00018 | 0.437 |
LIG_SH3_3 | 373 | 379 | PF00018 | 0.584 |
LIG_SH3_3 | 63 | 69 | PF00018 | 0.489 |
LIG_SUMO_SIM_anti_2 | 249 | 254 | PF11976 | 0.407 |
LIG_SUMO_SIM_anti_2 | 89 | 97 | PF11976 | 0.359 |
LIG_SUMO_SIM_par_1 | 322 | 327 | PF11976 | 0.379 |
LIG_TRAF2_1 | 183 | 186 | PF00917 | 0.474 |
LIG_TRAF2_1 | 288 | 291 | PF00917 | 0.429 |
LIG_TRAF2_1 | 35 | 38 | PF00917 | 0.676 |
LIG_WRC_WIRS_1 | 111 | 116 | PF05994 | 0.549 |
LIG_WW_3 | 26 | 30 | PF00397 | 0.683 |
MOD_CDC14_SPxK_1 | 42 | 45 | PF00782 | 0.800 |
MOD_CDK_SPxK_1 | 217 | 223 | PF00069 | 0.380 |
MOD_CDK_SPxK_1 | 39 | 45 | PF00069 | 0.803 |
MOD_CDK_SPxxK_3 | 1 | 8 | PF00069 | 0.690 |
MOD_CK1_1 | 101 | 107 | PF00069 | 0.411 |
MOD_CK1_1 | 113 | 119 | PF00069 | 0.551 |
MOD_CK1_1 | 13 | 19 | PF00069 | 0.737 |
MOD_CK1_1 | 207 | 213 | PF00069 | 0.410 |
MOD_CK1_1 | 345 | 351 | PF00069 | 0.506 |
MOD_CK2_1 | 285 | 291 | PF00069 | 0.489 |
MOD_CK2_1 | 31 | 37 | PF00069 | 0.788 |
MOD_CK2_1 | 312 | 318 | PF00069 | 0.510 |
MOD_GlcNHglycan | 118 | 121 | PF01048 | 0.548 |
MOD_GlcNHglycan | 244 | 247 | PF01048 | 0.325 |
MOD_GlcNHglycan | 318 | 322 | PF01048 | 0.538 |
MOD_GlcNHglycan | 344 | 347 | PF01048 | 0.514 |
MOD_GlcNHglycan | 416 | 419 | PF01048 | 0.571 |
MOD_GlcNHglycan | 61 | 64 | PF01048 | 0.659 |
MOD_GlcNHglycan | 98 | 101 | PF01048 | 0.368 |
MOD_GSK3_1 | 109 | 116 | PF00069 | 0.379 |
MOD_GSK3_1 | 242 | 249 | PF00069 | 0.345 |
MOD_GSK3_1 | 285 | 292 | PF00069 | 0.363 |
MOD_GSK3_1 | 29 | 36 | PF00069 | 0.743 |
MOD_GSK3_1 | 44 | 51 | PF00069 | 0.602 |
MOD_GSK3_1 | 52 | 59 | PF00069 | 0.781 |
MOD_GSK3_1 | 98 | 105 | PF00069 | 0.420 |
MOD_N-GLC_1 | 116 | 121 | PF02516 | 0.585 |
MOD_N-GLC_1 | 299 | 304 | PF02516 | 0.383 |
MOD_N-GLC_1 | 419 | 424 | PF02516 | 0.627 |
MOD_N-GLC_1 | 75 | 80 | PF02516 | 0.498 |
MOD_NEK2_1 | 132 | 137 | PF00069 | 0.339 |
MOD_NEK2_1 | 242 | 247 | PF00069 | 0.355 |
MOD_NEK2_1 | 269 | 274 | PF00069 | 0.309 |
MOD_NEK2_1 | 299 | 304 | PF00069 | 0.498 |
MOD_NEK2_1 | 342 | 347 | PF00069 | 0.482 |
MOD_PIKK_1 | 154 | 160 | PF00454 | 0.354 |
MOD_PIKK_1 | 207 | 213 | PF00454 | 0.515 |
MOD_PIKK_1 | 44 | 50 | PF00454 | 0.632 |
MOD_PKA_1 | 29 | 35 | PF00069 | 0.629 |
MOD_PKA_1 | 412 | 418 | PF00069 | 0.516 |
MOD_PKA_2 | 13 | 19 | PF00069 | 0.542 |
MOD_PKA_2 | 137 | 143 | PF00069 | 0.501 |
MOD_PKA_2 | 204 | 210 | PF00069 | 0.457 |
MOD_PKA_2 | 242 | 248 | PF00069 | 0.332 |
MOD_PKA_2 | 29 | 35 | PF00069 | 0.581 |
MOD_PKA_2 | 327 | 333 | PF00069 | 0.461 |
MOD_PKA_2 | 44 | 50 | PF00069 | 0.481 |
MOD_Plk_1 | 132 | 138 | PF00069 | 0.392 |
MOD_Plk_1 | 299 | 305 | PF00069 | 0.394 |
MOD_Plk_1 | 317 | 323 | PF00069 | 0.426 |
MOD_Plk_1 | 337 | 343 | PF00069 | 0.592 |
MOD_Plk_1 | 89 | 95 | PF00069 | 0.469 |
MOD_Plk_2-3 | 327 | 333 | PF00069 | 0.365 |
MOD_Plk_4 | 102 | 108 | PF00069 | 0.296 |
MOD_Plk_4 | 193 | 199 | PF00069 | 0.337 |
MOD_Plk_4 | 246 | 252 | PF00069 | 0.306 |
MOD_Plk_4 | 327 | 333 | PF00069 | 0.449 |
MOD_Plk_4 | 61 | 67 | PF00069 | 0.495 |
MOD_Plk_4 | 89 | 95 | PF00069 | 0.410 |
MOD_ProDKin_1 | 1 | 7 | PF00069 | 0.658 |
MOD_ProDKin_1 | 165 | 171 | PF00069 | 0.323 |
MOD_ProDKin_1 | 217 | 223 | PF00069 | 0.380 |
MOD_ProDKin_1 | 39 | 45 | PF00069 | 0.699 |
MOD_SUMO_rev_2 | 235 | 242 | PF00179 | 0.437 |
MOD_SUMO_rev_2 | 371 | 376 | PF00179 | 0.555 |
MOD_SUMO_rev_2 | 4 | 10 | PF00179 | 0.691 |
TRG_ENDOCYTIC_2 | 111 | 114 | PF00928 | 0.529 |
TRG_ER_diArg_1 | 199 | 201 | PF00400 | 0.409 |
TRG_ER_diArg_1 | 241 | 244 | PF00400 | 0.327 |
TRG_ER_diArg_1 | 259 | 261 | PF00400 | 0.368 |
TRG_ER_diArg_1 | 28 | 30 | PF00400 | 0.626 |
TRG_ER_diArg_1 | 381 | 383 | PF00400 | 0.642 |
TRG_NLS_Bipartite_1 | 401 | 416 | PF00514 | 0.445 |
TRG_NLS_MonoExtN_4 | 123 | 128 | PF00514 | 0.596 |
TRG_NLS_MonoExtN_4 | 237 | 244 | PF00514 | 0.424 |
TRG_Pf-PMV_PEXEL_1 | 200 | 204 | PF00026 | 0.396 |
TRG_Pf-PMV_PEXEL_1 | 367 | 371 | PF00026 | 0.686 |
TRG_Pf-PMV_PEXEL_1 | 382 | 386 | PF00026 | 0.480 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PAN3 | Leptomonas seymouri | 82% | 99% |
A0A0S4JG99 | Bodo saltans | 54% | 100% |
A0A1X0NS84 | Trypanosomatidae | 52% | 100% |
A0A3R7P067 | Trypanosoma rangeli | 54% | 100% |
A0A3S5H7T0 | Leishmania donovani | 96% | 100% |
A4HKW8 | Leishmania braziliensis | 84% | 99% |
A4I8E8 | Leishmania infantum | 95% | 100% |
D0AAS5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 52% | 100% |
E9B3A6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
Q32KV4 | Bos taurus | 28% | 100% |
Q6AY43 | Rattus norvegicus | 28% | 100% |
Q7SXY4 | Danio rerio | 29% | 100% |
Q7XA07 | Chlamydomonas reinhardtii | 24% | 100% |
Q8K0T2 | Mus musculus | 30% | 100% |
Q8TCX1 | Homo sapiens | 26% | 100% |