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: 1, no: 10 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0031974 | membrane-enclosed lumen | 2 | 1 |
GO:0031981 | nuclear lumen | 5 | 1 |
GO:0032838 | plasma membrane bounded cell projection cytoplasm | 4 | 1 |
GO:0043233 | organelle lumen | 3 | 1 |
GO:0070013 | intracellular organelle lumen | 4 | 1 |
GO:0097014 | ciliary plasm | 5 | 1 |
GO:0099568 | cytoplasmic region | 3 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
GO:0005875 | microtubule associated complex | 2 | 3 |
GO:0030286 | dynein complex | 3 | 3 |
GO:0032991 | protein-containing complex | 1 | 3 |
GO:1902494 | catalytic complex | 2 | 3 |
Related structures:
AlphaFold database: E9B760
Term | Name | Level | Count |
---|---|---|---|
GO:0007017 | microtubule-based process | 2 | 3 |
GO:0007018 | microtubule-based movement | 3 | 3 |
GO:0009987 | cellular process | 1 | 3 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003774 | cytoskeletal motor activity | 1 | 3 |
GO:0003777 | microtubule motor activity | 2 | 3 |
GO:0008569 | minus-end-directed microtubule motor activity | 3 | 3 |
GO:0140657 | ATP-dependent activity | 1 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 116 | 118 | PF00675 | 0.409 |
CLV_NRD_NRD_1 | 182 | 184 | PF00675 | 0.519 |
CLV_NRD_NRD_1 | 241 | 243 | PF00675 | 0.452 |
CLV_NRD_NRD_1 | 252 | 254 | PF00675 | 0.351 |
CLV_NRD_NRD_1 | 342 | 344 | PF00675 | 0.431 |
CLV_PCSK_KEX2_1 | 116 | 118 | PF00082 | 0.437 |
CLV_PCSK_KEX2_1 | 182 | 184 | PF00082 | 0.486 |
CLV_PCSK_KEX2_1 | 241 | 243 | PF00082 | 0.411 |
CLV_PCSK_KEX2_1 | 51 | 53 | PF00082 | 0.395 |
CLV_PCSK_PC1ET2_1 | 51 | 53 | PF00082 | 0.395 |
CLV_PCSK_SKI1_1 | 117 | 121 | PF00082 | 0.434 |
CLV_PCSK_SKI1_1 | 169 | 173 | PF00082 | 0.691 |
CLV_PCSK_SKI1_1 | 253 | 257 | PF00082 | 0.313 |
CLV_PCSK_SKI1_1 | 268 | 272 | PF00082 | 0.259 |
CLV_PCSK_SKI1_1 | 275 | 279 | PF00082 | 0.279 |
DOC_CYCLIN_RxL_1 | 163 | 173 | PF00134 | 0.515 |
DOC_CYCLIN_yCln2_LP_2 | 132 | 138 | PF00134 | 0.502 |
DOC_MAPK_MEF2A_6 | 121 | 130 | PF00069 | 0.347 |
DOC_PP2B_PxIxI_1 | 30 | 36 | PF00149 | 0.491 |
DOC_USP7_MATH_1 | 287 | 291 | PF00917 | 0.259 |
DOC_WW_Pin1_4 | 11 | 16 | PF00397 | 0.560 |
DOC_WW_Pin1_4 | 131 | 136 | PF00397 | 0.434 |
DOC_WW_Pin1_4 | 257 | 262 | PF00397 | 0.266 |
DOC_WW_Pin1_4 | 27 | 32 | PF00397 | 0.377 |
DOC_WW_Pin1_4 | 329 | 334 | PF00397 | 0.328 |
LIG_14-3-3_CanoR_1 | 24 | 32 | PF00244 | 0.288 |
LIG_14-3-3_CanoR_1 | 241 | 251 | PF00244 | 0.414 |
LIG_14-3-3_CanoR_1 | 275 | 281 | PF00244 | 0.351 |
LIG_AP2alpha_2 | 40 | 42 | PF02296 | 0.351 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.495 |
LIG_FHA_1 | 218 | 224 | PF00498 | 0.579 |
LIG_FHA_1 | 269 | 275 | PF00498 | 0.299 |
LIG_FHA_1 | 28 | 34 | PF00498 | 0.374 |
LIG_FHA_2 | 325 | 331 | PF00498 | 0.451 |
LIG_FHA_2 | 85 | 91 | PF00498 | 0.348 |
LIG_GBD_Chelix_1 | 100 | 108 | PF00786 | 0.531 |
LIG_LIR_Gen_1 | 159 | 167 | PF02991 | 0.638 |
LIG_LIR_Gen_1 | 315 | 325 | PF02991 | 0.318 |
LIG_LIR_Gen_1 | 40 | 49 | PF02991 | 0.370 |
LIG_LIR_Gen_1 | 72 | 78 | PF02991 | 0.389 |
LIG_LIR_Gen_1 | 82 | 91 | PF02991 | 0.272 |
LIG_LIR_Nem_3 | 10 | 16 | PF02991 | 0.465 |
LIG_LIR_Nem_3 | 103 | 108 | PF02991 | 0.521 |
LIG_LIR_Nem_3 | 118 | 123 | PF02991 | 0.295 |
LIG_LIR_Nem_3 | 159 | 164 | PF02991 | 0.593 |
LIG_LIR_Nem_3 | 315 | 320 | PF02991 | 0.357 |
LIG_LIR_Nem_3 | 40 | 45 | PF02991 | 0.374 |
LIG_LIR_Nem_3 | 72 | 76 | PF02991 | 0.366 |
LIG_LIR_Nem_3 | 82 | 86 | PF02991 | 0.299 |
LIG_LIR_Nem_3 | 94 | 100 | PF02991 | 0.364 |
LIG_MYND_1 | 111 | 115 | PF01753 | 0.452 |
LIG_Pex14_2 | 120 | 124 | PF04695 | 0.330 |
LIG_Pex14_2 | 140 | 144 | PF04695 | 0.555 |
LIG_SH2_CRK | 105 | 109 | PF00017 | 0.560 |
LIG_SH2_PTP2 | 73 | 76 | PF00017 | 0.361 |
LIG_SH2_SRC | 73 | 76 | PF00017 | 0.361 |
LIG_SH2_STAP1 | 9 | 13 | PF00017 | 0.317 |
LIG_SH2_STAT5 | 18 | 21 | PF00017 | 0.504 |
LIG_SH2_STAT5 | 338 | 341 | PF00017 | 0.428 |
LIG_SH2_STAT5 | 47 | 50 | PF00017 | 0.474 |
LIG_SH2_STAT5 | 73 | 76 | PF00017 | 0.372 |
LIG_SH2_STAT5 | 85 | 88 | PF00017 | 0.304 |
LIG_SH2_STAT5 | 9 | 12 | PF00017 | 0.376 |
LIG_SH2_STAT5 | 96 | 99 | PF00017 | 0.506 |
LIG_SH3_3 | 123 | 129 | PF00018 | 0.467 |
LIG_SH3_3 | 133 | 139 | PF00018 | 0.446 |
LIG_SH3_3 | 147 | 153 | PF00018 | 0.457 |
LIG_TYR_ITIM | 205 | 210 | PF00017 | 0.501 |
LIG_WRC_WIRS_1 | 56 | 61 | PF05994 | 0.457 |
MOD_CDC14_SPxK_1 | 14 | 17 | PF00782 | 0.403 |
MOD_CDK_SPxK_1 | 11 | 17 | PF00069 | 0.417 |
MOD_CK1_1 | 219 | 225 | PF00069 | 0.492 |
MOD_CK1_1 | 273 | 279 | PF00069 | 0.331 |
MOD_CK1_1 | 7 | 13 | PF00069 | 0.335 |
MOD_CK2_1 | 186 | 192 | PF00069 | 0.520 |
MOD_CK2_1 | 242 | 248 | PF00069 | 0.432 |
MOD_CK2_1 | 315 | 321 | PF00069 | 0.469 |
MOD_GlcNHglycan | 172 | 175 | PF01048 | 0.692 |
MOD_GlcNHglycan | 201 | 204 | PF01048 | 0.494 |
MOD_GlcNHglycan | 245 | 248 | PF01048 | 0.300 |
MOD_GlcNHglycan | 53 | 56 | PF01048 | 0.391 |
MOD_GSK3_1 | 186 | 193 | PF00069 | 0.520 |
MOD_GSK3_1 | 23 | 30 | PF00069 | 0.537 |
MOD_GSK3_1 | 324 | 331 | PF00069 | 0.455 |
MOD_GSK3_1 | 51 | 58 | PF00069 | 0.480 |
MOD_GSK3_1 | 7 | 14 | PF00069 | 0.536 |
MOD_N-GLC_1 | 7 | 12 | PF02516 | 0.451 |
MOD_NEK2_1 | 124 | 129 | PF00069 | 0.490 |
MOD_NEK2_1 | 144 | 149 | PF00069 | 0.452 |
MOD_NEK2_1 | 270 | 275 | PF00069 | 0.411 |
MOD_NEK2_2 | 167 | 172 | PF00069 | 0.604 |
MOD_PKA_1 | 51 | 57 | PF00069 | 0.358 |
MOD_PKA_2 | 151 | 157 | PF00069 | 0.610 |
MOD_PKA_2 | 186 | 192 | PF00069 | 0.520 |
MOD_PKA_2 | 199 | 205 | PF00069 | 0.474 |
MOD_PKA_2 | 23 | 29 | PF00069 | 0.294 |
MOD_PKA_2 | 287 | 293 | PF00069 | 0.259 |
MOD_PKA_2 | 51 | 57 | PF00069 | 0.472 |
MOD_Plk_1 | 167 | 173 | PF00069 | 0.510 |
MOD_Plk_1 | 216 | 222 | PF00069 | 0.511 |
MOD_Plk_2-3 | 188 | 194 | PF00069 | 0.517 |
MOD_Plk_4 | 145 | 151 | PF00069 | 0.386 |
MOD_Plk_4 | 167 | 173 | PF00069 | 0.510 |
MOD_Plk_4 | 92 | 98 | PF00069 | 0.473 |
MOD_ProDKin_1 | 11 | 17 | PF00069 | 0.565 |
MOD_ProDKin_1 | 131 | 137 | PF00069 | 0.435 |
MOD_ProDKin_1 | 257 | 263 | PF00069 | 0.266 |
MOD_ProDKin_1 | 27 | 33 | PF00069 | 0.370 |
MOD_ProDKin_1 | 329 | 335 | PF00069 | 0.318 |
MOD_SUMO_for_1 | 224 | 227 | PF00179 | 0.539 |
MOD_SUMO_rev_2 | 340 | 346 | PF00179 | 0.446 |
TRG_AP2beta_CARGO_1 | 315 | 324 | PF09066 | 0.305 |
TRG_ENDOCYTIC_2 | 105 | 108 | PF00928 | 0.565 |
TRG_ENDOCYTIC_2 | 207 | 210 | PF00928 | 0.611 |
TRG_ENDOCYTIC_2 | 73 | 76 | PF00928 | 0.372 |
TRG_ER_diArg_1 | 115 | 117 | PF00400 | 0.399 |
TRG_ER_diArg_1 | 240 | 242 | PF00400 | 0.331 |
TRG_NES_CRM1_1 | 269 | 283 | PF08389 | 0.331 |
TRG_Pf-PMV_PEXEL_1 | 106 | 110 | PF00026 | 0.473 |
TRG_Pf-PMV_PEXEL_1 | 214 | 218 | PF00026 | 0.648 |
TRG_Pf-PMV_PEXEL_1 | 253 | 257 | PF00026 | 0.366 |
TRG_Pf-PMV_PEXEL_1 | 307 | 311 | PF00026 | 0.411 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PEG4 | Leptomonas seymouri | 72% | 100% |
A0A0S4JP67 | Bodo saltans | 45% | 93% |
A0A1X0P5J8 | Trypanosomatidae | 49% | 100% |
A0A3Q8IIK7 | Leishmania donovani | 94% | 100% |
A0A3R7N649 | Trypanosoma rangeli | 47% | 100% |
A4HNJ5 | Leishmania braziliensis | 83% | 100% |
A4IC52 | Leishmania infantum | 94% | 100% |
C9ZYC2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 47% | 100% |
E9AG07 | Leishmania major | 93% | 100% |
V5BYP5 | Trypanosoma cruzi | 46% | 92% |