Uncharacterized Protein, Uncharacterized
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:0005929 | cilium | 4 | 6 |
GO:0042995 | cell projection | 2 | 6 |
GO:0043226 | organelle | 2 | 6 |
GO:0043227 | membrane-bounded organelle | 3 | 6 |
GO:0110165 | cellular anatomical entity | 1 | 6 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 6 |
Related structures:
AlphaFold database: A4I3L2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 183 | 185 | PF00675 | 0.460 |
CLV_NRD_NRD_1 | 289 | 291 | PF00675 | 0.429 |
CLV_NRD_NRD_1 | 324 | 326 | PF00675 | 0.470 |
CLV_NRD_NRD_1 | 50 | 52 | PF00675 | 0.679 |
CLV_NRD_NRD_1 | 91 | 93 | PF00675 | 0.691 |
CLV_PCSK_KEX2_1 | 183 | 185 | PF00082 | 0.460 |
CLV_PCSK_KEX2_1 | 289 | 291 | PF00082 | 0.429 |
CLV_PCSK_KEX2_1 | 324 | 326 | PF00082 | 0.413 |
CLV_PCSK_KEX2_1 | 50 | 52 | PF00082 | 0.679 |
CLV_PCSK_KEX2_1 | 91 | 93 | PF00082 | 0.661 |
CLV_PCSK_SKI1_1 | 289 | 293 | PF00082 | 0.355 |
CLV_PCSK_SKI1_1 | 35 | 39 | PF00082 | 0.621 |
DEG_APCC_DBOX_1 | 165 | 173 | PF00400 | 0.463 |
DOC_MAPK_gen_1 | 286 | 294 | PF00069 | 0.421 |
DOC_MAPK_gen_1 | 328 | 336 | PF00069 | 0.530 |
DOC_MAPK_MEF2A_6 | 218 | 227 | PF00069 | 0.419 |
DOC_MAPK_MEF2A_6 | 328 | 336 | PF00069 | 0.520 |
DOC_USP7_MATH_1 | 129 | 133 | PF00917 | 0.698 |
DOC_USP7_MATH_1 | 154 | 158 | PF00917 | 0.659 |
DOC_USP7_MATH_1 | 264 | 268 | PF00917 | 0.498 |
DOC_USP7_MATH_1 | 42 | 46 | PF00917 | 0.709 |
DOC_WW_Pin1_4 | 11 | 16 | PF00397 | 0.674 |
DOC_WW_Pin1_4 | 119 | 124 | PF00397 | 0.752 |
DOC_WW_Pin1_4 | 150 | 155 | PF00397 | 0.626 |
DOC_WW_Pin1_4 | 18 | 23 | PF00397 | 0.682 |
DOC_WW_Pin1_4 | 260 | 265 | PF00397 | 0.380 |
DOC_WW_Pin1_4 | 328 | 333 | PF00397 | 0.506 |
DOC_WW_Pin1_4 | 58 | 63 | PF00397 | 0.696 |
LIG_14-3-3_CanoR_1 | 128 | 134 | PF00244 | 0.604 |
LIG_14-3-3_CanoR_1 | 166 | 170 | PF00244 | 0.424 |
LIG_14-3-3_CanoR_1 | 176 | 181 | PF00244 | 0.367 |
LIG_14-3-3_CanoR_1 | 43 | 47 | PF00244 | 0.623 |
LIG_Actin_WH2_2 | 287 | 304 | PF00022 | 0.498 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.637 |
LIG_deltaCOP1_diTrp_1 | 72 | 77 | PF00928 | 0.602 |
LIG_FHA_1 | 222 | 228 | PF00498 | 0.420 |
LIG_FHA_1 | 273 | 279 | PF00498 | 0.436 |
LIG_FHA_1 | 329 | 335 | PF00498 | 0.520 |
LIG_FHA_1 | 77 | 83 | PF00498 | 0.660 |
LIG_FHA_2 | 229 | 235 | PF00498 | 0.422 |
LIG_FHA_2 | 36 | 42 | PF00498 | 0.619 |
LIG_LIR_Gen_1 | 234 | 243 | PF02991 | 0.422 |
LIG_LIR_Nem_3 | 234 | 238 | PF02991 | 0.411 |
LIG_PDZ_Class_1 | 345 | 350 | PF00595 | 0.567 |
LIG_SH2_GRB2like | 235 | 238 | PF00017 | 0.342 |
LIG_SH2_PTP2 | 235 | 238 | PF00017 | 0.408 |
LIG_SH2_SRC | 214 | 217 | PF00017 | 0.453 |
LIG_SH2_STAT5 | 173 | 176 | PF00017 | 0.451 |
LIG_SH2_STAT5 | 214 | 217 | PF00017 | 0.595 |
LIG_SH2_STAT5 | 229 | 232 | PF00017 | 0.427 |
LIG_SH2_STAT5 | 235 | 238 | PF00017 | 0.352 |
LIG_SH3_3 | 117 | 123 | PF00018 | 0.820 |
LIG_SH3_3 | 12 | 18 | PF00018 | 0.641 |
LIG_SH3_3 | 131 | 137 | PF00018 | 0.533 |
LIG_SH3_3 | 222 | 228 | PF00018 | 0.420 |
LIG_SH3_3 | 77 | 83 | PF00018 | 0.511 |
LIG_SUMO_SIM_par_1 | 274 | 279 | PF11976 | 0.437 |
LIG_SUMO_SIM_par_1 | 331 | 338 | PF11976 | 0.544 |
LIG_SUMO_SIM_par_1 | 78 | 84 | PF11976 | 0.492 |
LIG_TRAF2_1 | 339 | 342 | PF00917 | 0.646 |
LIG_TYR_ITIM | 233 | 238 | PF00017 | 0.410 |
LIG_WW_3 | 66 | 70 | PF00397 | 0.641 |
MOD_CDC14_SPxK_1 | 155 | 158 | PF00782 | 0.594 |
MOD_CDK_SPK_2 | 119 | 124 | PF00069 | 0.624 |
MOD_CDK_SPK_2 | 18 | 23 | PF00069 | 0.620 |
MOD_CDK_SPxK_1 | 152 | 158 | PF00069 | 0.587 |
MOD_CDK_SPxxK_3 | 62 | 69 | PF00069 | 0.573 |
MOD_CK1_1 | 122 | 128 | PF00069 | 0.625 |
MOD_CK1_1 | 159 | 165 | PF00069 | 0.511 |
MOD_CK1_1 | 168 | 174 | PF00069 | 0.403 |
MOD_CK1_1 | 21 | 27 | PF00069 | 0.700 |
MOD_CK1_1 | 28 | 34 | PF00069 | 0.678 |
MOD_CK1_1 | 61 | 67 | PF00069 | 0.700 |
MOD_CK1_1 | 84 | 90 | PF00069 | 0.549 |
MOD_CK2_1 | 228 | 234 | PF00069 | 0.428 |
MOD_CK2_1 | 35 | 41 | PF00069 | 0.599 |
MOD_Cter_Amidation | 287 | 290 | PF01082 | 0.416 |
MOD_GlcNHglycan | 131 | 134 | PF01048 | 0.651 |
MOD_GlcNHglycan | 158 | 161 | PF01048 | 0.565 |
MOD_GlcNHglycan | 246 | 249 | PF01048 | 0.569 |
MOD_GlcNHglycan | 266 | 269 | PF01048 | 0.527 |
MOD_GlcNHglycan | 30 | 33 | PF01048 | 0.711 |
MOD_GlcNHglycan | 52 | 55 | PF01048 | 0.816 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.636 |
MOD_GSK3_1 | 123 | 130 | PF00069 | 0.618 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.633 |
MOD_GSK3_1 | 161 | 168 | PF00069 | 0.398 |
MOD_GSK3_1 | 172 | 179 | PF00069 | 0.400 |
MOD_GSK3_1 | 21 | 28 | PF00069 | 0.673 |
MOD_GSK3_1 | 244 | 251 | PF00069 | 0.639 |
MOD_GSK3_1 | 260 | 267 | PF00069 | 0.574 |
MOD_GSK3_1 | 272 | 279 | PF00069 | 0.442 |
MOD_GSK3_1 | 324 | 331 | PF00069 | 0.443 |
MOD_GSK3_1 | 341 | 348 | PF00069 | 0.570 |
MOD_GSK3_1 | 58 | 65 | PF00069 | 0.656 |
MOD_GSK3_1 | 81 | 88 | PF00069 | 0.517 |
MOD_N-GLC_2 | 237 | 239 | PF02516 | 0.343 |
MOD_NEK2_1 | 172 | 177 | PF00069 | 0.435 |
MOD_NEK2_1 | 76 | 81 | PF00069 | 0.595 |
MOD_PIKK_1 | 93 | 99 | PF00454 | 0.590 |
MOD_PKA_1 | 324 | 330 | PF00069 | 0.442 |
MOD_PKA_1 | 50 | 56 | PF00069 | 0.678 |
MOD_PKA_2 | 127 | 133 | PF00069 | 0.604 |
MOD_PKA_2 | 165 | 171 | PF00069 | 0.477 |
MOD_PKA_2 | 210 | 216 | PF00069 | 0.457 |
MOD_PKA_2 | 324 | 330 | PF00069 | 0.437 |
MOD_PKA_2 | 42 | 48 | PF00069 | 0.659 |
MOD_PKA_2 | 50 | 56 | PF00069 | 0.667 |
MOD_PKA_2 | 85 | 91 | PF00069 | 0.668 |
MOD_PKB_1 | 312 | 320 | PF00069 | 0.377 |
MOD_Plk_1 | 115 | 121 | PF00069 | 0.631 |
MOD_Plk_1 | 276 | 282 | PF00069 | 0.448 |
MOD_Plk_4 | 107 | 113 | PF00069 | 0.567 |
MOD_Plk_4 | 137 | 143 | PF00069 | 0.611 |
MOD_Plk_4 | 210 | 216 | PF00069 | 0.457 |
MOD_Plk_4 | 221 | 227 | PF00069 | 0.415 |
MOD_Plk_4 | 4 | 10 | PF00069 | 0.631 |
MOD_Plk_4 | 76 | 82 | PF00069 | 0.547 |
MOD_ProDKin_1 | 11 | 17 | PF00069 | 0.674 |
MOD_ProDKin_1 | 119 | 125 | PF00069 | 0.751 |
MOD_ProDKin_1 | 150 | 156 | PF00069 | 0.630 |
MOD_ProDKin_1 | 18 | 24 | PF00069 | 0.683 |
MOD_ProDKin_1 | 260 | 266 | PF00069 | 0.390 |
MOD_ProDKin_1 | 328 | 334 | PF00069 | 0.511 |
MOD_ProDKin_1 | 58 | 64 | PF00069 | 0.692 |
TRG_DiLeu_BaLyEn_6 | 185 | 190 | PF01217 | 0.412 |
TRG_DiLeu_BaLyEn_6 | 287 | 292 | PF01217 | 0.336 |
TRG_ENDOCYTIC_2 | 235 | 238 | PF00928 | 0.408 |
TRG_ER_diArg_1 | 182 | 184 | PF00400 | 0.456 |
TRG_ER_diArg_1 | 289 | 291 | PF00400 | 0.429 |
TRG_ER_diArg_1 | 323 | 325 | PF00400 | 0.414 |
TRG_ER_diArg_1 | 90 | 92 | PF00400 | 0.660 |
TRG_Pf-PMV_PEXEL_1 | 188 | 192 | PF00026 | 0.468 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IDS7 | Leishmania donovani | 100% | 100% |
A4HGI0 | Leishmania braziliensis | 64% | 96% |
E9AZV2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
Q4Q8D3 | Leishmania major | 88% | 100% |