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: 5 |
NetGPI | no | yes: 0, no: 5 |
Term | Name | Level | Count |
---|---|---|---|
GO:0035869 | ciliary transition zone | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q9U1D2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 145 | 149 | PF00656 | 0.603 |
CLV_C14_Caspase3-7 | 328 | 332 | PF00656 | 0.537 |
CLV_C14_Caspase3-7 | 335 | 339 | PF00656 | 0.610 |
CLV_C14_Caspase3-7 | 45 | 49 | PF00656 | 0.649 |
CLV_NRD_NRD_1 | 128 | 130 | PF00675 | 0.685 |
CLV_NRD_NRD_1 | 272 | 274 | PF00675 | 0.548 |
CLV_NRD_NRD_1 | 458 | 460 | PF00675 | 0.621 |
CLV_NRD_NRD_1 | 66 | 68 | PF00675 | 0.640 |
CLV_NRD_NRD_1 | 99 | 101 | PF00675 | 0.687 |
CLV_PCSK_FUR_1 | 57 | 61 | PF00082 | 0.729 |
CLV_PCSK_KEX2_1 | 123 | 125 | PF00082 | 0.746 |
CLV_PCSK_KEX2_1 | 128 | 130 | PF00082 | 0.718 |
CLV_PCSK_KEX2_1 | 272 | 274 | PF00082 | 0.551 |
CLV_PCSK_KEX2_1 | 458 | 460 | PF00082 | 0.621 |
CLV_PCSK_KEX2_1 | 59 | 61 | PF00082 | 0.729 |
CLV_PCSK_KEX2_1 | 66 | 68 | PF00082 | 0.652 |
CLV_PCSK_PC1ET2_1 | 123 | 125 | PF00082 | 0.710 |
CLV_PCSK_PC1ET2_1 | 59 | 61 | PF00082 | 0.729 |
CLV_PCSK_PC7_1 | 124 | 130 | PF00082 | 0.635 |
CLV_PCSK_SKI1_1 | 212 | 216 | PF00082 | 0.635 |
CLV_PCSK_SKI1_1 | 378 | 382 | PF00082 | 0.565 |
CLV_PCSK_SKI1_1 | 70 | 74 | PF00082 | 0.696 |
DEG_SCF_TRCP1_1 | 403 | 409 | PF00400 | 0.600 |
DEG_SPOP_SBC_1 | 203 | 207 | PF00917 | 0.625 |
DEG_SPOP_SBC_1 | 231 | 235 | PF00917 | 0.722 |
DEG_SPOP_SBC_1 | 90 | 94 | PF00917 | 0.733 |
DOC_CYCLIN_RxL_1 | 209 | 217 | PF00134 | 0.635 |
DOC_MAPK_DCC_7 | 272 | 281 | PF00069 | 0.614 |
DOC_MAPK_DCC_7 | 378 | 388 | PF00069 | 0.543 |
DOC_MAPK_MEF2A_6 | 272 | 281 | PF00069 | 0.614 |
DOC_MAPK_MEF2A_6 | 374 | 383 | PF00069 | 0.569 |
DOC_PP2B_LxvP_1 | 156 | 159 | PF13499 | 0.674 |
DOC_PP2B_PxIxI_1 | 276 | 282 | PF00149 | 0.595 |
DOC_USP7_MATH_1 | 138 | 142 | PF00917 | 0.593 |
DOC_USP7_MATH_1 | 232 | 236 | PF00917 | 0.716 |
DOC_USP7_MATH_1 | 312 | 316 | PF00917 | 0.589 |
DOC_USP7_MATH_1 | 475 | 479 | PF00917 | 0.538 |
DOC_USP7_MATH_1 | 90 | 94 | PF00917 | 0.732 |
DOC_WW_Pin1_4 | 134 | 139 | PF00397 | 0.736 |
DOC_WW_Pin1_4 | 149 | 154 | PF00397 | 0.577 |
DOC_WW_Pin1_4 | 157 | 162 | PF00397 | 0.602 |
DOC_WW_Pin1_4 | 284 | 289 | PF00397 | 0.587 |
DOC_WW_Pin1_4 | 38 | 43 | PF00397 | 0.669 |
DOC_WW_Pin1_4 | 406 | 411 | PF00397 | 0.602 |
DOC_WW_Pin1_4 | 95 | 100 | PF00397 | 0.692 |
LIG_14-3-3_CanoR_1 | 10 | 14 | PF00244 | 0.624 |
LIG_14-3-3_CanoR_1 | 174 | 179 | PF00244 | 0.652 |
LIG_14-3-3_CanoR_1 | 196 | 200 | PF00244 | 0.704 |
LIG_14-3-3_CanoR_1 | 202 | 210 | PF00244 | 0.659 |
LIG_14-3-3_CanoR_1 | 367 | 376 | PF00244 | 0.583 |
LIG_14-3-3_CanoR_1 | 438 | 445 | PF00244 | 0.534 |
LIG_14-3-3_CanoR_1 | 57 | 63 | PF00244 | 0.682 |
LIG_Actin_WH2_2 | 437 | 454 | PF00022 | 0.585 |
LIG_APCC_ABBA_1 | 437 | 442 | PF00400 | 0.579 |
LIG_FHA_1 | 158 | 164 | PF00498 | 0.710 |
LIG_FHA_1 | 205 | 211 | PF00498 | 0.656 |
LIG_FHA_1 | 276 | 282 | PF00498 | 0.565 |
LIG_FHA_2 | 477 | 483 | PF00498 | 0.622 |
LIG_LIR_Apic_2 | 12 | 16 | PF02991 | 0.619 |
LIG_LIR_Apic_2 | 283 | 288 | PF02991 | 0.633 |
LIG_LIR_Apic_2 | 490 | 496 | PF02991 | 0.633 |
LIG_PDZ_Wminus1_1 | 506 | 508 | PF00595 | 0.549 |
LIG_Pex14_1 | 13 | 17 | PF04695 | 0.622 |
LIG_SH2_CRK | 285 | 289 | PF00017 | 0.647 |
LIG_SH2_CRK | 493 | 497 | PF00017 | 0.599 |
LIG_SH2_STAT5 | 421 | 424 | PF00017 | 0.583 |
LIG_SH3_1 | 101 | 107 | PF00018 | 0.607 |
LIG_SH3_2 | 104 | 109 | PF14604 | 0.603 |
LIG_SH3_3 | 101 | 107 | PF00018 | 0.716 |
LIG_SH3_3 | 110 | 116 | PF00018 | 0.656 |
LIG_SH3_3 | 156 | 162 | PF00018 | 0.705 |
LIG_SH3_3 | 197 | 203 | PF00018 | 0.693 |
LIG_SH3_3 | 404 | 410 | PF00018 | 0.606 |
LIG_SH3_3 | 433 | 439 | PF00018 | 0.662 |
LIG_SH3_3 | 75 | 81 | PF00018 | 0.712 |
LIG_TRAF2_1 | 360 | 363 | PF00917 | 0.574 |
LIG_TRAF2_1 | 479 | 482 | PF00917 | 0.596 |
LIG_TRFH_1 | 258 | 262 | PF08558 | 0.671 |
MOD_CDC14_SPxK_1 | 98 | 101 | PF00782 | 0.689 |
MOD_CDK_SPK_2 | 95 | 100 | PF00069 | 0.692 |
MOD_CDK_SPxK_1 | 95 | 101 | PF00069 | 0.693 |
MOD_CK1_1 | 134 | 140 | PF00069 | 0.696 |
MOD_CK1_1 | 177 | 183 | PF00069 | 0.698 |
MOD_CK1_1 | 188 | 194 | PF00069 | 0.637 |
MOD_CK1_1 | 204 | 210 | PF00069 | 0.537 |
MOD_CK1_1 | 217 | 223 | PF00069 | 0.677 |
MOD_CK1_1 | 233 | 239 | PF00069 | 0.659 |
MOD_CK1_1 | 41 | 47 | PF00069 | 0.705 |
MOD_CK2_1 | 357 | 363 | PF00069 | 0.614 |
MOD_CK2_1 | 412 | 418 | PF00069 | 0.602 |
MOD_CK2_1 | 476 | 482 | PF00069 | 0.609 |
MOD_Cter_Amidation | 126 | 129 | PF01082 | 0.689 |
MOD_GlcNHglycan | 140 | 143 | PF01048 | 0.724 |
MOD_GlcNHglycan | 170 | 173 | PF01048 | 0.716 |
MOD_GlcNHglycan | 176 | 179 | PF01048 | 0.646 |
MOD_GlcNHglycan | 226 | 229 | PF01048 | 0.696 |
MOD_GlcNHglycan | 30 | 33 | PF01048 | 0.670 |
MOD_GlcNHglycan | 318 | 321 | PF01048 | 0.622 |
MOD_GlcNHglycan | 403 | 406 | PF01048 | 0.595 |
MOD_GlcNHglycan | 414 | 417 | PF01048 | 0.480 |
MOD_GSK3_1 | 134 | 141 | PF00069 | 0.681 |
MOD_GSK3_1 | 174 | 181 | PF00069 | 0.632 |
MOD_GSK3_1 | 185 | 192 | PF00069 | 0.651 |
MOD_GSK3_1 | 226 | 233 | PF00069 | 0.679 |
MOD_GSK3_1 | 235 | 242 | PF00069 | 0.682 |
MOD_GSK3_1 | 256 | 263 | PF00069 | 0.671 |
MOD_GSK3_1 | 312 | 319 | PF00069 | 0.600 |
MOD_GSK3_1 | 338 | 345 | PF00069 | 0.632 |
MOD_GSK3_1 | 40 | 47 | PF00069 | 0.667 |
MOD_GSK3_1 | 401 | 408 | PF00069 | 0.564 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.731 |
MOD_NEK2_1 | 214 | 219 | PF00069 | 0.623 |
MOD_NEK2_2 | 256 | 261 | PF00069 | 0.657 |
MOD_PIKK_1 | 226 | 232 | PF00454 | 0.672 |
MOD_PKA_1 | 123 | 129 | PF00069 | 0.712 |
MOD_PKA_2 | 123 | 129 | PF00069 | 0.712 |
MOD_PKA_2 | 195 | 201 | PF00069 | 0.668 |
MOD_PKA_2 | 217 | 223 | PF00069 | 0.714 |
MOD_PKA_2 | 224 | 230 | PF00069 | 0.734 |
MOD_PKA_2 | 260 | 266 | PF00069 | 0.628 |
MOD_PKA_2 | 9 | 15 | PF00069 | 0.622 |
MOD_Plk_2-3 | 338 | 344 | PF00069 | 0.633 |
MOD_Plk_4 | 325 | 331 | PF00069 | 0.428 |
MOD_ProDKin_1 | 134 | 140 | PF00069 | 0.734 |
MOD_ProDKin_1 | 149 | 155 | PF00069 | 0.579 |
MOD_ProDKin_1 | 157 | 163 | PF00069 | 0.603 |
MOD_ProDKin_1 | 284 | 290 | PF00069 | 0.580 |
MOD_ProDKin_1 | 38 | 44 | PF00069 | 0.670 |
MOD_ProDKin_1 | 406 | 412 | PF00069 | 0.599 |
MOD_ProDKin_1 | 95 | 101 | PF00069 | 0.693 |
TRG_ENDOCYTIC_2 | 349 | 352 | PF00928 | 0.634 |
TRG_ER_diArg_1 | 128 | 130 | PF00400 | 0.685 |
TRG_ER_diArg_1 | 222 | 225 | PF00400 | 0.657 |
TRG_ER_diArg_1 | 271 | 273 | PF00400 | 0.578 |
TRG_ER_diArg_1 | 294 | 297 | PF00400 | 0.570 |
TRG_ER_diArg_1 | 458 | 460 | PF00400 | 0.621 |
TRG_ER_diArg_1 | 65 | 67 | PF00400 | 0.652 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S5H5D8 | Leishmania donovani | 84% | 97% |
A4H411 | Leishmania braziliensis | 68% | 100% |
A4HS94 | Leishmania infantum | 84% | 100% |
E9AK78 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 79% | 100% |