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: 14 |
NetGPI | no | yes: 0, no: 14 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005930 | axoneme | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: A4HBW2
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 | 147 | 151 | PF00656 | 0.405 |
CLV_NRD_NRD_1 | 126 | 128 | PF00675 | 0.366 |
CLV_NRD_NRD_1 | 168 | 170 | PF00675 | 0.373 |
CLV_NRD_NRD_1 | 217 | 219 | PF00675 | 0.252 |
CLV_NRD_NRD_1 | 263 | 265 | PF00675 | 0.332 |
CLV_NRD_NRD_1 | 57 | 59 | PF00675 | 0.530 |
CLV_NRD_NRD_1 | 99 | 101 | PF00675 | 0.465 |
CLV_PCSK_KEX2_1 | 126 | 128 | PF00082 | 0.358 |
CLV_PCSK_KEX2_1 | 168 | 170 | PF00082 | 0.386 |
CLV_PCSK_KEX2_1 | 217 | 219 | PF00082 | 0.252 |
CLV_PCSK_KEX2_1 | 263 | 265 | PF00082 | 0.340 |
CLV_PCSK_KEX2_1 | 292 | 294 | PF00082 | 0.302 |
CLV_PCSK_KEX2_1 | 298 | 300 | PF00082 | 0.258 |
CLV_PCSK_KEX2_1 | 57 | 59 | PF00082 | 0.565 |
CLV_PCSK_KEX2_1 | 93 | 95 | PF00082 | 0.379 |
CLV_PCSK_KEX2_1 | 99 | 101 | PF00082 | 0.427 |
CLV_PCSK_PC1ET2_1 | 292 | 294 | PF00082 | 0.279 |
CLV_PCSK_PC1ET2_1 | 298 | 300 | PF00082 | 0.222 |
CLV_PCSK_PC1ET2_1 | 93 | 95 | PF00082 | 0.379 |
CLV_PCSK_SKI1_1 | 176 | 180 | PF00082 | 0.251 |
CLV_PCSK_SKI1_1 | 189 | 193 | PF00082 | 0.368 |
CLV_PCSK_SKI1_1 | 198 | 202 | PF00082 | 0.275 |
CLV_PCSK_SKI1_1 | 217 | 221 | PF00082 | 0.232 |
CLV_PCSK_SKI1_1 | 229 | 233 | PF00082 | 0.268 |
CLV_PCSK_SKI1_1 | 94 | 98 | PF00082 | 0.373 |
CLV_Separin_Metazoa | 186 | 190 | PF03568 | 0.366 |
DEG_SPOP_SBC_1 | 11 | 15 | PF00917 | 0.481 |
DOC_CKS1_1 | 122 | 127 | PF01111 | 0.308 |
DOC_CYCLIN_RxL_1 | 173 | 182 | PF00134 | 0.249 |
DOC_CYCLIN_RxL_1 | 91 | 101 | PF00134 | 0.398 |
DOC_CYCLIN_yCln2_LP_2 | 306 | 312 | PF00134 | 0.585 |
DOC_MAPK_MEF2A_6 | 109 | 117 | PF00069 | 0.443 |
DOC_MAPK_MEF2A_6 | 198 | 205 | PF00069 | 0.283 |
DOC_MAPK_NFAT4_5 | 198 | 206 | PF00069 | 0.303 |
DOC_MAPK_RevD_3 | 113 | 127 | PF00069 | 0.366 |
DOC_MAPK_RevD_3 | 42 | 58 | PF00069 | 0.421 |
DOC_PP2B_LxvP_1 | 306 | 309 | PF13499 | 0.489 |
DOC_PP4_FxxP_1 | 122 | 125 | PF00568 | 0.232 |
DOC_USP7_MATH_1 | 11 | 15 | PF00917 | 0.674 |
DOC_USP7_MATH_1 | 143 | 147 | PF00917 | 0.366 |
DOC_USP7_MATH_1 | 174 | 178 | PF00917 | 0.232 |
DOC_USP7_MATH_1 | 212 | 216 | PF00917 | 0.238 |
DOC_USP7_MATH_1 | 38 | 42 | PF00917 | 0.551 |
DOC_USP7_MATH_1 | 56 | 60 | PF00917 | 0.462 |
DOC_USP7_MATH_1 | 74 | 78 | PF00917 | 0.439 |
DOC_USP7_MATH_1 | 92 | 96 | PF00917 | 0.362 |
DOC_USP7_UBL2_3 | 236 | 240 | PF12436 | 0.366 |
DOC_USP7_UBL2_3 | 93 | 97 | PF12436 | 0.393 |
DOC_WW_Pin1_4 | 121 | 126 | PF00397 | 0.296 |
DOC_WW_Pin1_4 | 139 | 144 | PF00397 | 0.258 |
DOC_WW_Pin1_4 | 170 | 175 | PF00397 | 0.308 |
LIG_14-3-3_CanoR_1 | 12 | 20 | PF00244 | 0.522 |
LIG_14-3-3_CanoR_1 | 189 | 196 | PF00244 | 0.232 |
LIG_14-3-3_CanoR_1 | 57 | 66 | PF00244 | 0.399 |
LIG_14-3-3_CanoR_1 | 99 | 103 | PF00244 | 0.414 |
LIG_APCC_ABBA_1 | 203 | 208 | PF00400 | 0.249 |
LIG_FHA_1 | 131 | 137 | PF00498 | 0.365 |
LIG_FHA_1 | 170 | 176 | PF00498 | 0.376 |
LIG_LIR_Apic_2 | 120 | 125 | PF02991 | 0.232 |
LIG_PCNA_TLS_4 | 116 | 123 | PF02747 | 0.232 |
LIG_PCNA_yPIPBox_3 | 48 | 58 | PF02747 | 0.477 |
LIG_SH2_CRK | 83 | 87 | PF00017 | 0.353 |
LIG_SH2_NCK_1 | 83 | 87 | PF00017 | 0.336 |
LIG_SH2_PTP2 | 67 | 70 | PF00017 | 0.382 |
LIG_SH2_SRC | 67 | 70 | PF00017 | 0.499 |
LIG_SH2_SRC | 83 | 86 | PF00017 | 0.373 |
LIG_SH2_SRC | 87 | 90 | PF00017 | 0.391 |
LIG_SH2_STAT5 | 67 | 70 | PF00017 | 0.382 |
LIG_SH3_1 | 83 | 89 | PF00018 | 0.352 |
LIG_SH3_2 | 73 | 78 | PF14604 | 0.469 |
LIG_SH3_2 | 89 | 94 | PF14604 | 0.394 |
LIG_SH3_3 | 107 | 113 | PF00018 | 0.439 |
LIG_SH3_3 | 5 | 11 | PF00018 | 0.486 |
LIG_SH3_3 | 67 | 73 | PF00018 | 0.389 |
LIG_SH3_3 | 83 | 89 | PF00018 | 0.388 |
LIG_TRAF2_1 | 59 | 62 | PF00917 | 0.626 |
LIG_WRC_WIRS_1 | 119 | 124 | PF05994 | 0.232 |
MOD_CDC14_SPxK_1 | 173 | 176 | PF00782 | 0.308 |
MOD_CDK_SPK_2 | 121 | 126 | PF00069 | 0.304 |
MOD_CDK_SPxK_1 | 121 | 127 | PF00069 | 0.366 |
MOD_CDK_SPxK_1 | 170 | 176 | PF00069 | 0.308 |
MOD_CK1_1 | 121 | 127 | PF00069 | 0.307 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.513 |
MOD_CK1_1 | 37 | 43 | PF00069 | 0.661 |
MOD_CK2_1 | 264 | 270 | PF00069 | 0.322 |
MOD_CK2_1 | 56 | 62 | PF00069 | 0.511 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.683 |
MOD_GlcNHglycan | 23 | 26 | PF01048 | 0.566 |
MOD_GlcNHglycan | 35 | 39 | PF01048 | 0.730 |
MOD_GlcNHglycan | 40 | 43 | PF01048 | 0.717 |
MOD_GSK3_1 | 139 | 146 | PF00069 | 0.280 |
MOD_GSK3_1 | 170 | 177 | PF00069 | 0.317 |
MOD_GSK3_1 | 21 | 28 | PF00069 | 0.623 |
MOD_GSK3_1 | 30 | 37 | PF00069 | 0.681 |
MOD_N-GLC_1 | 29 | 34 | PF02516 | 0.521 |
MOD_NEK2_1 | 21 | 26 | PF00069 | 0.487 |
MOD_NEK2_1 | 219 | 224 | PF00069 | 0.268 |
MOD_NEK2_1 | 98 | 103 | PF00069 | 0.490 |
MOD_NEK2_2 | 92 | 97 | PF00069 | 0.395 |
MOD_PIKK_1 | 151 | 157 | PF00454 | 0.366 |
MOD_PKA_1 | 57 | 63 | PF00069 | 0.468 |
MOD_PKA_2 | 11 | 17 | PF00069 | 0.513 |
MOD_PKA_2 | 167 | 173 | PF00069 | 0.317 |
MOD_PKA_2 | 30 | 36 | PF00069 | 0.479 |
MOD_PKA_2 | 56 | 62 | PF00069 | 0.501 |
MOD_PKA_2 | 98 | 104 | PF00069 | 0.411 |
MOD_Plk_1 | 243 | 249 | PF00069 | 0.199 |
MOD_Plk_4 | 118 | 124 | PF00069 | 0.226 |
MOD_ProDKin_1 | 121 | 127 | PF00069 | 0.296 |
MOD_ProDKin_1 | 139 | 145 | PF00069 | 0.258 |
MOD_ProDKin_1 | 170 | 176 | PF00069 | 0.308 |
MOD_SUMO_for_1 | 232 | 235 | PF00179 | 0.232 |
MOD_SUMO_for_1 | 239 | 242 | PF00179 | 0.232 |
MOD_SUMO_for_1 | 291 | 294 | PF00179 | 0.249 |
TRG_DiLeu_BaEn_1 | 197 | 202 | PF01217 | 0.283 |
TRG_DiLeu_BaEn_1 | 274 | 279 | PF01217 | 0.232 |
TRG_ENDOCYTIC_2 | 67 | 70 | PF00928 | 0.368 |
TRG_ER_diArg_1 | 125 | 127 | PF00400 | 0.366 |
TRG_ER_diArg_1 | 217 | 219 | PF00400 | 0.462 |
TRG_ER_diArg_1 | 262 | 264 | PF00400 | 0.391 |
TRG_ER_diArg_1 | 56 | 58 | PF00400 | 0.627 |
TRG_ER_diArg_1 | 98 | 100 | PF00400 | 0.310 |
TRG_NES_CRM1_1 | 243 | 258 | PF08389 | 0.313 |
TRG_Pf-PMV_PEXEL_1 | 116 | 120 | PF00026 | 0.156 |
TRG_Pf-PMV_PEXEL_1 | 217 | 221 | PF00026 | 0.268 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3Q9 | Leptomonas seymouri | 74% | 100% |
A0A0S4J9S1 | Bodo saltans | 34% | 100% |
A0A0S4KGN7 | Bodo saltans | 57% | 100% |
A0A1X0NVG2 | Trypanosomatidae | 33% | 100% |
A0A1X0NXR5 | Trypanosomatidae | 61% | 100% |
A0A3Q8IC16 | Leishmania donovani | 32% | 100% |
A0A3Q8IM75 | Leishmania donovani | 34% | 100% |
A0A3R7KMX9 | Trypanosoma rangeli | 33% | 100% |
A0A3S7WWL7 | Leishmania donovani | 89% | 100% |
A0A422NWB3 | Trypanosoma rangeli | 59% | 100% |
A4I0S3 | Leishmania infantum | 32% | 100% |
A4I8Y3 | Leishmania infantum | 34% | 100% |
D0A1A2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 59% | 100% |
E9AGX0 | Leishmania infantum | 88% | 100% |
E9AIH0 | Leishmania braziliensis | 36% | 100% |
E9AV86 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 99% |
E9AWS5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 100% |
E9B3V2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 100% |
Q39604 | Chlamydomonas reinhardtii | 34% | 100% |
Q4QAP9 | Leishmania major | 35% | 100% |
Q4QC94 | Leishmania major | 88% | 100% |
Q4R3K5 | Macaca fascicularis | 32% | 100% |
Q9VGG6 | Drosophila melanogaster | 30% | 100% |
V5BR59 | Trypanosoma cruzi | 32% | 100% |