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: 5 |
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: 5 |
NetGPI | no | yes: 0, no: 5 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005813 | centrosome | 3 | 2 |
GO:0005815 | microtubule organizing center | 2 | 2 |
GO:0005930 | axoneme | 2 | 2 |
GO:0030992 | intraciliary transport particle B | 2 | 2 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0036064 | ciliary basal body | 3 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4QC32
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 2 |
GO:0006996 | organelle organization | 4 | 2 |
GO:0007017 | microtubule-based process | 2 | 2 |
GO:0007018 | microtubule-based movement | 3 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0010970 | transport along microtubule | 4 | 2 |
GO:0016043 | cellular component organization | 3 | 2 |
GO:0022607 | cellular component assembly | 4 | 2 |
GO:0030030 | cell projection organization | 4 | 2 |
GO:0030031 | cell projection assembly | 5 | 2 |
GO:0030705 | cytoskeleton-dependent intracellular transport | 4 | 2 |
GO:0031503 | protein-containing complex localization | 2 | 2 |
GO:0032886 | regulation of microtubule-based process | 4 | 2 |
GO:0033043 | regulation of organelle organization | 5 | 2 |
GO:0042073 | intraciliary transport | 3 | 2 |
GO:0044782 | cilium organization | 5 | 2 |
GO:0046907 | intracellular transport | 3 | 2 |
GO:0050789 | regulation of biological process | 2 | 2 |
GO:0050794 | regulation of cellular process | 3 | 2 |
GO:0051128 | regulation of cellular component organization | 4 | 2 |
GO:0051179 | localization | 1 | 2 |
GO:0051234 | establishment of localization | 2 | 2 |
GO:0051493 | regulation of cytoskeleton organization | 6 | 2 |
GO:0051641 | cellular localization | 2 | 2 |
GO:0051649 | establishment of localization in cell | 3 | 2 |
GO:0060271 | cilium assembly | 6 | 2 |
GO:0065007 | biological regulation | 1 | 2 |
GO:0070507 | regulation of microtubule cytoskeleton organization | 5 | 2 |
GO:0070925 | organelle assembly | 5 | 2 |
GO:0071840 | cellular component organization or biogenesis | 2 | 2 |
GO:0099111 | microtubule-based transport | 4 | 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 | 6 |
GO:0005515 | protein binding | 2 | 6 |
GO:0008017 | microtubule binding | 5 | 6 |
GO:0008092 | cytoskeletal protein binding | 3 | 6 |
GO:0015631 | tubulin binding | 4 | 6 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 400 | 404 | PF00656 | 0.636 |
CLV_C14_Caspase3-7 | 55 | 59 | PF00656 | 0.636 |
CLV_NRD_NRD_1 | 125 | 127 | PF00675 | 0.647 |
CLV_NRD_NRD_1 | 167 | 169 | PF00675 | 0.672 |
CLV_NRD_NRD_1 | 174 | 176 | PF00675 | 0.571 |
CLV_NRD_NRD_1 | 222 | 224 | PF00675 | 0.783 |
CLV_NRD_NRD_1 | 238 | 240 | PF00675 | 0.703 |
CLV_NRD_NRD_1 | 332 | 334 | PF00675 | 0.408 |
CLV_NRD_NRD_1 | 427 | 429 | PF00675 | 0.435 |
CLV_PCSK_FUR_1 | 164 | 168 | PF00082 | 0.748 |
CLV_PCSK_FUR_1 | 172 | 176 | PF00082 | 0.657 |
CLV_PCSK_KEX2_1 | 166 | 168 | PF00082 | 0.772 |
CLV_PCSK_KEX2_1 | 172 | 174 | PF00082 | 0.658 |
CLV_PCSK_KEX2_1 | 180 | 182 | PF00082 | 0.521 |
CLV_PCSK_KEX2_1 | 224 | 226 | PF00082 | 0.842 |
CLV_PCSK_KEX2_1 | 272 | 274 | PF00082 | 0.724 |
CLV_PCSK_KEX2_1 | 324 | 326 | PF00082 | 0.435 |
CLV_PCSK_KEX2_1 | 332 | 334 | PF00082 | 0.341 |
CLV_PCSK_KEX2_1 | 427 | 429 | PF00082 | 0.435 |
CLV_PCSK_PC1ET2_1 | 166 | 168 | PF00082 | 0.772 |
CLV_PCSK_PC1ET2_1 | 180 | 182 | PF00082 | 0.521 |
CLV_PCSK_PC1ET2_1 | 224 | 226 | PF00082 | 0.858 |
CLV_PCSK_PC1ET2_1 | 272 | 274 | PF00082 | 0.724 |
CLV_PCSK_PC1ET2_1 | 324 | 326 | PF00082 | 0.435 |
CLV_PCSK_PC7_1 | 168 | 174 | PF00082 | 0.762 |
CLV_PCSK_PC7_1 | 220 | 226 | PF00082 | 0.867 |
CLV_PCSK_SKI1_1 | 313 | 317 | PF00082 | 0.437 |
CLV_PCSK_SKI1_1 | 65 | 69 | PF00082 | 0.435 |
CLV_PCSK_SKI1_1 | 90 | 94 | PF00082 | 0.297 |
DEG_APCC_DBOX_1 | 377 | 385 | PF00400 | 0.636 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.688 |
DOC_MAPK_gen_1 | 65 | 71 | PF00069 | 0.636 |
DOC_MAPK_RevD_3 | 310 | 325 | PF00069 | 0.636 |
DOC_PP1_RVXF_1 | 66 | 72 | PF00149 | 0.636 |
DOC_USP7_MATH_1 | 115 | 119 | PF00917 | 0.621 |
DOC_USP7_MATH_1 | 142 | 146 | PF00917 | 0.865 |
DOC_USP7_MATH_1 | 234 | 238 | PF00917 | 0.861 |
DOC_USP7_UBL2_3 | 199 | 203 | PF12436 | 0.617 |
DOC_USP7_UBL2_3 | 20 | 24 | PF12436 | 0.552 |
DOC_USP7_UBL2_3 | 61 | 65 | PF12436 | 0.636 |
DOC_WW_Pin1_4 | 342 | 347 | PF00397 | 0.497 |
DOC_WW_Pin1_4 | 82 | 87 | PF00397 | 0.608 |
LIG_14-3-3_CanoR_1 | 427 | 434 | PF00244 | 0.636 |
LIG_Actin_WH2_2 | 445 | 461 | PF00022 | 0.636 |
LIG_BIR_III_2 | 260 | 264 | PF00653 | 0.845 |
LIG_FHA_1 | 101 | 107 | PF00498 | 0.608 |
LIG_FHA_1 | 20 | 26 | PF00498 | 0.636 |
LIG_FHA_1 | 226 | 232 | PF00498 | 0.785 |
LIG_FHA_1 | 246 | 252 | PF00498 | 0.855 |
LIG_FHA_1 | 301 | 307 | PF00498 | 0.715 |
LIG_FHA_1 | 404 | 410 | PF00498 | 0.636 |
LIG_FHA_1 | 453 | 459 | PF00498 | 0.636 |
LIG_FHA_2 | 158 | 164 | PF00498 | 0.738 |
LIG_FHA_2 | 188 | 194 | PF00498 | 0.647 |
LIG_FHA_2 | 196 | 202 | PF00498 | 0.723 |
LIG_FHA_2 | 276 | 282 | PF00498 | 0.771 |
LIG_FHA_2 | 6 | 12 | PF00498 | 0.636 |
LIG_LIR_Gen_1 | 105 | 115 | PF02991 | 0.636 |
LIG_LIR_Gen_1 | 286 | 295 | PF02991 | 0.790 |
LIG_LIR_Nem_3 | 105 | 110 | PF02991 | 0.636 |
LIG_LIR_Nem_3 | 286 | 291 | PF02991 | 0.785 |
LIG_PCNA_yPIPBox_3 | 7 | 16 | PF02747 | 0.636 |
LIG_SH2_STAT5 | 33 | 36 | PF00017 | 0.636 |
LIG_SH3_1 | 239 | 245 | PF00018 | 0.852 |
LIG_SH3_3 | 239 | 245 | PF00018 | 0.852 |
LIG_TRAF2_1 | 160 | 163 | PF00917 | 0.697 |
LIG_TRAF2_1 | 198 | 201 | PF00917 | 0.716 |
LIG_TRAF2_1 | 433 | 436 | PF00917 | 0.636 |
LIG_TRAF2_1 | 96 | 99 | PF00917 | 0.636 |
LIG_WRC_WIRS_1 | 38 | 43 | PF05994 | 0.580 |
LIG_WW_3 | 241 | 245 | PF00397 | 0.850 |
MOD_CK1_1 | 150 | 156 | PF00069 | 0.764 |
MOD_CK1_1 | 211 | 217 | PF00069 | 0.751 |
MOD_CK1_1 | 356 | 362 | PF00069 | 0.622 |
MOD_CK2_1 | 143 | 149 | PF00069 | 0.872 |
MOD_CK2_1 | 155 | 161 | PF00069 | 0.644 |
MOD_CK2_1 | 195 | 201 | PF00069 | 0.717 |
MOD_CK2_1 | 275 | 281 | PF00069 | 0.777 |
MOD_CK2_1 | 430 | 436 | PF00069 | 0.636 |
MOD_CK2_1 | 5 | 11 | PF00069 | 0.636 |
MOD_Cter_Amidation | 270 | 273 | PF01082 | 0.700 |
MOD_GlcNHglycan | 117 | 120 | PF01048 | 0.685 |
MOD_GlcNHglycan | 128 | 131 | PF01048 | 0.605 |
MOD_GlcNHglycan | 149 | 152 | PF01048 | 0.782 |
MOD_GlcNHglycan | 210 | 213 | PF01048 | 0.752 |
MOD_GlcNHglycan | 236 | 239 | PF01048 | 0.861 |
MOD_GlcNHglycan | 58 | 61 | PF01048 | 0.380 |
MOD_GSK3_1 | 143 | 150 | PF00069 | 0.772 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.732 |
MOD_GSK3_1 | 230 | 237 | PF00069 | 0.806 |
MOD_GSK3_1 | 352 | 359 | PF00069 | 0.636 |
MOD_NEK2_1 | 42 | 47 | PF00069 | 0.581 |
MOD_NEK2_1 | 458 | 463 | PF00069 | 0.619 |
MOD_NEK2_1 | 472 | 477 | PF00069 | 0.453 |
MOD_PIKK_1 | 5 | 11 | PF00454 | 0.636 |
MOD_PKA_1 | 126 | 132 | PF00069 | 0.656 |
MOD_PKA_1 | 147 | 153 | PF00069 | 0.766 |
MOD_PKA_1 | 224 | 230 | PF00069 | 0.824 |
MOD_PKA_1 | 427 | 433 | PF00069 | 0.636 |
MOD_PKA_2 | 224 | 230 | PF00069 | 0.824 |
MOD_PKA_2 | 427 | 433 | PF00069 | 0.636 |
MOD_PKA_2 | 458 | 464 | PF00069 | 0.636 |
MOD_PKA_2 | 56 | 62 | PF00069 | 0.486 |
MOD_PKB_1 | 223 | 231 | PF00069 | 0.747 |
MOD_Plk_1 | 430 | 436 | PF00069 | 0.636 |
MOD_Plk_2-3 | 277 | 283 | PF00069 | 0.845 |
MOD_Plk_4 | 37 | 43 | PF00069 | 0.626 |
MOD_Plk_4 | 458 | 464 | PF00069 | 0.636 |
MOD_Plk_4 | 472 | 478 | PF00069 | 0.470 |
MOD_ProDKin_1 | 342 | 348 | PF00069 | 0.497 |
MOD_ProDKin_1 | 82 | 88 | PF00069 | 0.608 |
MOD_SUMO_for_1 | 323 | 326 | PF00179 | 0.469 |
MOD_SUMO_rev_2 | 146 | 156 | PF00179 | 0.762 |
MOD_SUMO_rev_2 | 196 | 205 | PF00179 | 0.639 |
MOD_SUMO_rev_2 | 293 | 300 | PF00179 | 0.815 |
MOD_SUMO_rev_2 | 308 | 315 | PF00179 | 0.458 |
MOD_SUMO_rev_2 | 58 | 67 | PF00179 | 0.636 |
TRG_DiLeu_BaEn_1 | 379 | 384 | PF01217 | 0.608 |
TRG_ER_diArg_1 | 172 | 175 | PF00400 | 0.759 |
TRG_NES_CRM1_1 | 400 | 415 | PF08389 | 0.636 |
TRG_NLS_MonoExtC_3 | 271 | 277 | PF00514 | 0.701 |
TRG_NLS_MonoExtN_4 | 269 | 276 | PF00514 | 0.714 |
TRG_Pf-PMV_PEXEL_1 | 32 | 36 | PF00026 | 0.435 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7WWV8 | Leishmania donovani | 95% | 100% |
A4HC10 | Leishmania braziliensis | 80% | 99% |
A4HZM1 | Leishmania infantum | 94% | 100% |
E9AVE7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |