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 | 1 |
GO:0005815 | microtubule organizing center | 2 | 1 |
GO:0005930 | axoneme | 2 | 1 |
GO:0030992 | intraciliary transport particle B | 2 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0036064 | ciliary basal body | 3 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HC10
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 1 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0007017 | microtubule-based process | 2 | 1 |
GO:0007018 | microtubule-based movement | 3 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0010970 | transport along microtubule | 4 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0022607 | cellular component assembly | 4 | 1 |
GO:0030030 | cell projection organization | 4 | 1 |
GO:0030031 | cell projection assembly | 5 | 1 |
GO:0030705 | cytoskeleton-dependent intracellular transport | 4 | 1 |
GO:0031503 | protein-containing complex localization | 2 | 1 |
GO:0032886 | regulation of microtubule-based process | 4 | 1 |
GO:0033043 | regulation of organelle organization | 5 | 1 |
GO:0042073 | intraciliary transport | 3 | 1 |
GO:0044782 | cilium organization | 5 | 1 |
GO:0046907 | intracellular transport | 3 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0051128 | regulation of cellular component organization | 4 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
GO:0051493 | regulation of cytoskeleton organization | 6 | 1 |
GO:0051641 | cellular localization | 2 | 1 |
GO:0051649 | establishment of localization in cell | 3 | 1 |
GO:0060271 | cilium assembly | 6 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0070507 | regulation of microtubule cytoskeleton organization | 5 | 1 |
GO:0070925 | organelle assembly | 5 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:0099111 | microtubule-based transport | 4 | 1 |
GO:0120031 | plasma membrane bounded cell projection assembly | 6 | 1 |
GO:0120036 | plasma membrane bounded cell projection organization | 5 | 1 |
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 | 236 | 240 | PF00656 | 0.634 |
CLV_C14_Caspase3-7 | 407 | 411 | PF00656 | 0.546 |
CLV_C14_Caspase3-7 | 55 | 59 | PF00656 | 0.546 |
CLV_NRD_NRD_1 | 177 | 179 | PF00675 | 0.639 |
CLV_NRD_NRD_1 | 184 | 186 | PF00675 | 0.546 |
CLV_NRD_NRD_1 | 190 | 192 | PF00675 | 0.483 |
CLV_NRD_NRD_1 | 248 | 250 | PF00675 | 0.621 |
CLV_NRD_NRD_1 | 342 | 344 | PF00675 | 0.415 |
CLV_NRD_NRD_1 | 434 | 436 | PF00675 | 0.346 |
CLV_PCSK_FUR_1 | 182 | 186 | PF00082 | 0.559 |
CLV_PCSK_KEX2_1 | 176 | 178 | PF00082 | 0.637 |
CLV_PCSK_KEX2_1 | 182 | 184 | PF00082 | 0.562 |
CLV_PCSK_KEX2_1 | 189 | 191 | PF00082 | 0.483 |
CLV_PCSK_KEX2_1 | 234 | 236 | PF00082 | 0.718 |
CLV_PCSK_KEX2_1 | 282 | 284 | PF00082 | 0.728 |
CLV_PCSK_KEX2_1 | 334 | 336 | PF00082 | 0.398 |
CLV_PCSK_KEX2_1 | 342 | 344 | PF00082 | 0.374 |
CLV_PCSK_KEX2_1 | 434 | 436 | PF00082 | 0.346 |
CLV_PCSK_PC1ET2_1 | 176 | 178 | PF00082 | 0.637 |
CLV_PCSK_PC1ET2_1 | 189 | 191 | PF00082 | 0.483 |
CLV_PCSK_PC1ET2_1 | 234 | 236 | PF00082 | 0.728 |
CLV_PCSK_PC1ET2_1 | 282 | 284 | PF00082 | 0.728 |
CLV_PCSK_PC1ET2_1 | 334 | 336 | PF00082 | 0.346 |
CLV_PCSK_PC7_1 | 178 | 184 | PF00082 | 0.626 |
CLV_PCSK_PC7_1 | 185 | 191 | PF00082 | 0.544 |
CLV_PCSK_PC7_1 | 230 | 236 | PF00082 | 0.732 |
CLV_PCSK_SKI1_1 | 112 | 116 | PF00082 | 0.234 |
CLV_PCSK_SKI1_1 | 158 | 162 | PF00082 | 0.560 |
CLV_PCSK_SKI1_1 | 164 | 168 | PF00082 | 0.524 |
CLV_PCSK_SKI1_1 | 199 | 203 | PF00082 | 0.499 |
CLV_PCSK_SKI1_1 | 323 | 327 | PF00082 | 0.346 |
CLV_PCSK_SKI1_1 | 65 | 69 | PF00082 | 0.346 |
DEG_APCC_DBOX_1 | 384 | 392 | PF00400 | 0.546 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.564 |
DOC_CYCLIN_yCln2_LP_2 | 143 | 149 | PF00134 | 0.578 |
DOC_MAPK_gen_1 | 65 | 71 | PF00069 | 0.546 |
DOC_MAPK_RevD_3 | 320 | 335 | PF00069 | 0.546 |
DOC_PP1_RVXF_1 | 66 | 72 | PF00149 | 0.546 |
DOC_PP2B_LxvP_1 | 143 | 146 | PF13499 | 0.575 |
DOC_USP7_MATH_1 | 153 | 157 | PF00917 | 0.747 |
DOC_USP7_MATH_1 | 244 | 248 | PF00917 | 0.733 |
DOC_USP7_MATH_1 | 273 | 277 | PF00917 | 0.579 |
DOC_USP7_MATH_1 | 344 | 348 | PF00917 | 0.441 |
DOC_USP7_MATH_1 | 89 | 93 | PF00917 | 0.537 |
DOC_USP7_UBL2_3 | 129 | 133 | PF12436 | 0.496 |
DOC_USP7_UBL2_3 | 20 | 24 | PF12436 | 0.494 |
DOC_USP7_UBL2_3 | 61 | 65 | PF12436 | 0.546 |
DOC_WW_Pin1_4 | 114 | 119 | PF00397 | 0.580 |
DOC_WW_Pin1_4 | 137 | 142 | PF00397 | 0.567 |
DOC_WW_Pin1_4 | 82 | 87 | PF00397 | 0.531 |
LIG_14-3-3_CanoR_1 | 152 | 160 | PF00244 | 0.571 |
LIG_14-3-3_CanoR_1 | 434 | 441 | PF00244 | 0.546 |
LIG_Actin_WH2_2 | 452 | 468 | PF00022 | 0.561 |
LIG_BIR_III_2 | 270 | 274 | PF00653 | 0.719 |
LIG_FHA_1 | 101 | 107 | PF00498 | 0.529 |
LIG_FHA_1 | 20 | 26 | PF00498 | 0.546 |
LIG_FHA_1 | 256 | 262 | PF00498 | 0.693 |
LIG_FHA_1 | 311 | 317 | PF00498 | 0.706 |
LIG_FHA_1 | 411 | 417 | PF00498 | 0.546 |
LIG_FHA_1 | 460 | 466 | PF00498 | 0.546 |
LIG_FHA_1 | 478 | 484 | PF00498 | 0.414 |
LIG_FHA_2 | 198 | 204 | PF00498 | 0.617 |
LIG_FHA_2 | 206 | 212 | PF00498 | 0.673 |
LIG_FHA_2 | 402 | 408 | PF00498 | 0.451 |
LIG_FHA_2 | 438 | 444 | PF00498 | 0.434 |
LIG_FHA_2 | 6 | 12 | PF00498 | 0.546 |
LIG_LIR_Gen_1 | 105 | 114 | PF02991 | 0.595 |
LIG_LIR_Gen_1 | 297 | 305 | PF02991 | 0.670 |
LIG_LIR_Nem_3 | 105 | 110 | PF02991 | 0.595 |
LIG_LIR_Nem_3 | 297 | 301 | PF02991 | 0.653 |
LIG_PCNA_yPIPBox_3 | 7 | 16 | PF02747 | 0.546 |
LIG_SH2_STAT5 | 33 | 36 | PF00017 | 0.546 |
LIG_SH3_1 | 249 | 255 | PF00018 | 0.719 |
LIG_SH3_3 | 249 | 255 | PF00018 | 0.719 |
LIG_TRAF2_1 | 208 | 211 | PF00917 | 0.725 |
LIG_TRAF2_1 | 440 | 443 | PF00917 | 0.546 |
LIG_TRAF2_1 | 96 | 99 | PF00917 | 0.546 |
LIG_UBA3_1 | 106 | 112 | PF00899 | 0.434 |
LIG_WW_3 | 251 | 255 | PF00397 | 0.718 |
MOD_CDK_SPxxK_3 | 114 | 121 | PF00069 | 0.551 |
MOD_CK1_1 | 205 | 211 | PF00069 | 0.591 |
MOD_CK1_1 | 368 | 374 | PF00069 | 0.544 |
MOD_CK1_1 | 60 | 66 | PF00069 | 0.434 |
MOD_CK2_1 | 153 | 159 | PF00069 | 0.729 |
MOD_CK2_1 | 167 | 173 | PF00069 | 0.534 |
MOD_CK2_1 | 197 | 203 | PF00069 | 0.587 |
MOD_CK2_1 | 205 | 211 | PF00069 | 0.691 |
MOD_CK2_1 | 219 | 225 | PF00069 | 0.589 |
MOD_CK2_1 | 437 | 443 | PF00069 | 0.598 |
MOD_CK2_1 | 5 | 11 | PF00069 | 0.546 |
MOD_Cter_Amidation | 280 | 283 | PF01082 | 0.721 |
MOD_GlcNHglycan | 122 | 125 | PF01048 | 0.576 |
MOD_GlcNHglycan | 129 | 132 | PF01048 | 0.669 |
MOD_GlcNHglycan | 143 | 146 | PF01048 | 0.672 |
MOD_GlcNHglycan | 246 | 249 | PF01048 | 0.820 |
MOD_GlcNHglycan | 370 | 373 | PF01048 | 0.234 |
MOD_GSK3_1 | 137 | 144 | PF00069 | 0.597 |
MOD_GSK3_1 | 197 | 204 | PF00069 | 0.589 |
MOD_GSK3_1 | 205 | 212 | PF00069 | 0.692 |
MOD_GSK3_1 | 215 | 222 | PF00069 | 0.610 |
MOD_GSK3_1 | 240 | 247 | PF00069 | 0.731 |
MOD_GSK3_1 | 359 | 366 | PF00069 | 0.601 |
MOD_GSK3_1 | 370 | 377 | PF00069 | 0.473 |
MOD_GSK3_1 | 418 | 425 | PF00069 | 0.434 |
MOD_GSK3_1 | 56 | 63 | PF00069 | 0.451 |
MOD_NEK2_1 | 401 | 406 | PF00069 | 0.455 |
MOD_NEK2_1 | 42 | 47 | PF00069 | 0.545 |
MOD_NEK2_1 | 459 | 464 | PF00069 | 0.573 |
MOD_NEK2_1 | 465 | 470 | PF00069 | 0.622 |
MOD_NEK2_1 | 479 | 484 | PF00069 | 0.459 |
MOD_NEK2_1 | 57 | 62 | PF00069 | 0.435 |
MOD_PIKK_1 | 158 | 164 | PF00454 | 0.555 |
MOD_PIKK_1 | 210 | 216 | PF00454 | 0.578 |
MOD_PIKK_1 | 422 | 428 | PF00454 | 0.434 |
MOD_PIKK_1 | 5 | 11 | PF00454 | 0.546 |
MOD_PK_1 | 234 | 240 | PF00069 | 0.574 |
MOD_PKA_1 | 234 | 240 | PF00069 | 0.707 |
MOD_PKA_1 | 434 | 440 | PF00069 | 0.546 |
MOD_PKA_2 | 120 | 126 | PF00069 | 0.488 |
MOD_PKA_2 | 151 | 157 | PF00069 | 0.575 |
MOD_PKA_2 | 234 | 240 | PF00069 | 0.707 |
MOD_PKA_2 | 368 | 374 | PF00069 | 0.434 |
MOD_PKA_2 | 42 | 48 | PF00069 | 0.447 |
MOD_PKA_2 | 434 | 440 | PF00069 | 0.546 |
MOD_PKA_2 | 465 | 471 | PF00069 | 0.593 |
MOD_PKA_2 | 89 | 95 | PF00069 | 0.486 |
MOD_Plk_1 | 197 | 203 | PF00069 | 0.493 |
MOD_Plk_1 | 437 | 443 | PF00069 | 0.546 |
MOD_Plk_2-3 | 287 | 293 | PF00069 | 0.701 |
MOD_Plk_4 | 273 | 279 | PF00069 | 0.606 |
MOD_Plk_4 | 37 | 43 | PF00069 | 0.546 |
MOD_Plk_4 | 465 | 471 | PF00069 | 0.632 |
MOD_Plk_4 | 479 | 485 | PF00069 | 0.469 |
MOD_ProDKin_1 | 114 | 120 | PF00069 | 0.582 |
MOD_ProDKin_1 | 137 | 143 | PF00069 | 0.569 |
MOD_ProDKin_1 | 82 | 88 | PF00069 | 0.531 |
MOD_SUMO_rev_2 | 287 | 296 | PF00179 | 0.573 |
MOD_SUMO_rev_2 | 303 | 310 | PF00179 | 0.648 |
MOD_SUMO_rev_2 | 318 | 325 | PF00179 | 0.429 |
MOD_SUMO_rev_2 | 58 | 67 | PF00179 | 0.546 |
TRG_DiLeu_BaEn_1 | 321 | 326 | PF01217 | 0.434 |
TRG_DiLeu_BaEn_1 | 386 | 391 | PF01217 | 0.529 |
TRG_ER_diArg_1 | 182 | 185 | PF00400 | 0.623 |
TRG_NES_CRM1_1 | 407 | 422 | PF08389 | 0.632 |
TRG_NLS_MonoExtC_3 | 281 | 287 | PF00514 | 0.726 |
TRG_NLS_MonoExtN_4 | 279 | 286 | PF00514 | 0.723 |
TRG_Pf-PMV_PEXEL_1 | 32 | 36 | PF00026 | 0.346 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7WWV8 | Leishmania donovani | 79% | 100% |
A4HZM1 | Leishmania infantum | 79% | 100% |
E9AVE7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 77% | 100% |
Q4QC32 | Leishmania major | 80% | 98% |