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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005856 | cytoskeleton | 5 | 1 |
GO:0005886 | plasma membrane | 3 | 1 |
GO:0016020 | membrane | 2 | 1 |
GO:0030863 | cortical cytoskeleton | 6 | 1 |
GO:0030864 | cortical actin cytoskeleton | 7 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4I5T2
Term | Name | Level | Count |
---|---|---|---|
GO:0008064 | regulation of actin polymerization or depolymerization | 6 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0030832 | regulation of actin filament length | 5 | 1 |
GO:0030833 | regulation of actin filament polymerization | 7 | 1 |
GO:0032271 | regulation of protein polymerization | 6 | 1 |
GO:0032535 | regulation of cellular component size | 4 | 1 |
GO:0032956 | regulation of actin cytoskeleton organization | 5 | 1 |
GO:0032970 | regulation of actin filament-based process | 4 | 1 |
GO:0033043 | regulation of organelle organization | 5 | 1 |
GO:0043254 | regulation of protein-containing complex assembly | 5 | 1 |
GO:0044087 | regulation of cellular component biogenesis | 4 | 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:0051493 | regulation of cytoskeleton organization | 6 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0065008 | regulation of biological quality | 2 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:0090066 | regulation of anatomical structure size | 3 | 1 |
GO:0110053 | regulation of actin filament organization | 6 | 1 |
GO:1902903 | regulation of supramolecular fiber organization | 5 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003779 | actin binding | 4 | 10 |
GO:0005488 | binding | 1 | 10 |
GO:0005515 | protein binding | 2 | 10 |
GO:0008092 | cytoskeletal protein binding | 3 | 10 |
GO:0044877 | protein-containing complex binding | 2 | 1 |
GO:0051015 | actin filament binding | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 12 | 16 | PF00656 | 0.302 |
CLV_NRD_NRD_1 | 147 | 149 | PF00675 | 0.577 |
CLV_NRD_NRD_1 | 245 | 247 | PF00675 | 0.261 |
CLV_NRD_NRD_1 | 310 | 312 | PF00675 | 0.496 |
CLV_PCSK_FUR_1 | 145 | 149 | PF00082 | 0.565 |
CLV_PCSK_KEX2_1 | 144 | 146 | PF00082 | 0.540 |
CLV_PCSK_KEX2_1 | 147 | 149 | PF00082 | 0.580 |
CLV_PCSK_KEX2_1 | 245 | 247 | PF00082 | 0.262 |
CLV_PCSK_KEX2_1 | 310 | 312 | PF00082 | 0.618 |
CLV_PCSK_KEX2_1 | 41 | 43 | PF00082 | 0.340 |
CLV_PCSK_KEX2_1 | 59 | 61 | PF00082 | 0.307 |
CLV_PCSK_PC1ET2_1 | 144 | 146 | PF00082 | 0.515 |
CLV_PCSK_PC1ET2_1 | 41 | 43 | PF00082 | 0.366 |
CLV_PCSK_PC1ET2_1 | 59 | 61 | PF00082 | 0.295 |
CLV_PCSK_SKI1_1 | 182 | 186 | PF00082 | 0.478 |
CLV_PCSK_SKI1_1 | 246 | 250 | PF00082 | 0.278 |
CLV_PCSK_SKI1_1 | 301 | 305 | PF00082 | 0.369 |
DEG_Kelch_Keap1_1 | 236 | 241 | PF01344 | 0.476 |
DEG_SCF_TRCP1_1 | 105 | 110 | PF00400 | 0.426 |
DOC_CKS1_1 | 304 | 309 | PF01111 | 0.424 |
DOC_CYCLIN_yCln2_LP_2 | 354 | 360 | PF00134 | 0.515 |
DOC_MAPK_gen_1 | 166 | 176 | PF00069 | 0.483 |
DOC_MAPK_gen_1 | 349 | 358 | PF00069 | 0.585 |
DOC_MAPK_gen_1 | 41 | 48 | PF00069 | 0.313 |
DOC_MAPK_MEF2A_6 | 147 | 156 | PF00069 | 0.604 |
DOC_MAPK_RevD_3 | 230 | 246 | PF00069 | 0.435 |
DOC_PP1_RVXF_1 | 232 | 238 | PF00149 | 0.458 |
DOC_PP1_RVXF_1 | 244 | 251 | PF00149 | 0.398 |
DOC_PP2B_LxvP_1 | 354 | 357 | PF13499 | 0.522 |
DOC_PP4_FxxP_1 | 304 | 307 | PF00568 | 0.404 |
DOC_USP7_MATH_1 | 34 | 38 | PF00917 | 0.452 |
DOC_USP7_MATH_1 | 380 | 384 | PF00917 | 0.609 |
DOC_USP7_MATH_1 | 53 | 57 | PF00917 | 0.268 |
DOC_WW_Pin1_4 | 169 | 174 | PF00397 | 0.509 |
DOC_WW_Pin1_4 | 274 | 279 | PF00397 | 0.524 |
DOC_WW_Pin1_4 | 303 | 308 | PF00397 | 0.404 |
DOC_WW_Pin1_4 | 375 | 380 | PF00397 | 0.620 |
LIG_14-3-3_CanoR_1 | 147 | 152 | PF00244 | 0.579 |
LIG_14-3-3_CanoR_1 | 182 | 188 | PF00244 | 0.265 |
LIG_14-3-3_CanoR_1 | 234 | 238 | PF00244 | 0.415 |
LIG_14-3-3_CanoR_1 | 331 | 335 | PF00244 | 0.368 |
LIG_14-3-3_CanoR_1 | 347 | 357 | PF00244 | 0.441 |
LIG_APCC_ABBA_1 | 127 | 132 | PF00400 | 0.394 |
LIG_BRCT_BRCA1_1 | 105 | 109 | PF00533 | 0.459 |
LIG_BRCT_BRCA1_1 | 321 | 325 | PF00533 | 0.460 |
LIG_BRCT_BRCA1_1 | 36 | 40 | PF00533 | 0.447 |
LIG_BRCT_BRCA1_1 | 87 | 91 | PF00533 | 0.388 |
LIG_deltaCOP1_diTrp_1 | 225 | 233 | PF00928 | 0.451 |
LIG_FHA_1 | 178 | 184 | PF00498 | 0.419 |
LIG_FHA_1 | 338 | 344 | PF00498 | 0.635 |
LIG_FHA_1 | 349 | 355 | PF00498 | 0.690 |
LIG_FHA_1 | 387 | 393 | PF00498 | 0.331 |
LIG_FHA_1 | 70 | 76 | PF00498 | 0.379 |
LIG_FHA_2 | 163 | 169 | PF00498 | 0.586 |
LIG_FHA_2 | 304 | 310 | PF00498 | 0.534 |
LIG_GBD_Chelix_1 | 400 | 408 | PF00786 | 0.271 |
LIG_LIR_Apic_2 | 302 | 307 | PF02991 | 0.380 |
LIG_LIR_Gen_1 | 193 | 200 | PF02991 | 0.444 |
LIG_LIR_Gen_1 | 88 | 98 | PF02991 | 0.440 |
LIG_LIR_Nem_3 | 193 | 199 | PF02991 | 0.444 |
LIG_LIR_Nem_3 | 227 | 233 | PF02991 | 0.428 |
LIG_LIR_Nem_3 | 88 | 94 | PF02991 | 0.432 |
LIG_LYPXL_S_1 | 268 | 272 | PF13949 | 0.294 |
LIG_LYPXL_yS_3 | 269 | 272 | PF13949 | 0.494 |
LIG_PCNA_yPIPBox_3 | 209 | 220 | PF02747 | 0.413 |
LIG_PDZ_Class_3 | 403 | 408 | PF00595 | 0.276 |
LIG_Pex14_2 | 233 | 237 | PF04695 | 0.494 |
LIG_SH2_PTP2 | 50 | 53 | PF00017 | 0.387 |
LIG_SH2_STAP1 | 281 | 285 | PF00017 | 0.431 |
LIG_SH2_STAT5 | 284 | 287 | PF00017 | 0.415 |
LIG_SH2_STAT5 | 47 | 50 | PF00017 | 0.311 |
LIG_SH3_3 | 157 | 163 | PF00018 | 0.622 |
LIG_SH3_3 | 167 | 173 | PF00018 | 0.537 |
LIG_SH3_3 | 354 | 360 | PF00018 | 0.627 |
LIG_SUMO_SIM_anti_2 | 387 | 394 | PF11976 | 0.380 |
LIG_SUMO_SIM_par_1 | 171 | 177 | PF11976 | 0.461 |
LIG_TRAF2_1 | 165 | 168 | PF00917 | 0.533 |
LIG_TRAF2_1 | 224 | 227 | PF00917 | 0.518 |
LIG_TRAF2_1 | 385 | 388 | PF00917 | 0.381 |
LIG_UBA3_1 | 216 | 221 | PF00899 | 0.438 |
MOD_CDK_SPxxK_3 | 303 | 310 | PF00069 | 0.419 |
MOD_CK1_1 | 177 | 183 | PF00069 | 0.569 |
MOD_CK1_1 | 366 | 372 | PF00069 | 0.601 |
MOD_CK1_1 | 90 | 96 | PF00069 | 0.313 |
MOD_CK2_1 | 162 | 168 | PF00069 | 0.684 |
MOD_CK2_1 | 169 | 175 | PF00069 | 0.659 |
MOD_CK2_1 | 198 | 204 | PF00069 | 0.433 |
MOD_CK2_1 | 235 | 241 | PF00069 | 0.476 |
MOD_CK2_1 | 330 | 336 | PF00069 | 0.458 |
MOD_CK2_1 | 382 | 388 | PF00069 | 0.452 |
MOD_Cter_Amidation | 145 | 148 | PF01082 | 0.534 |
MOD_DYRK1A_RPxSP_1 | 169 | 173 | PF00069 | 0.528 |
MOD_GlcNHglycan | 105 | 108 | PF01048 | 0.611 |
MOD_GlcNHglycan | 175 | 179 | PF01048 | 0.351 |
MOD_GlcNHglycan | 301 | 304 | PF01048 | 0.502 |
MOD_GlcNHglycan | 36 | 39 | PF01048 | 0.484 |
MOD_GlcNHglycan | 366 | 369 | PF01048 | 0.669 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.440 |
MOD_GSK3_1 | 200 | 207 | PF00069 | 0.511 |
MOD_GSK3_1 | 299 | 306 | PF00069 | 0.474 |
MOD_GSK3_1 | 319 | 326 | PF00069 | 0.458 |
MOD_GSK3_1 | 348 | 355 | PF00069 | 0.691 |
MOD_GSK3_1 | 366 | 373 | PF00069 | 0.561 |
MOD_GSK3_1 | 382 | 389 | PF00069 | 0.577 |
MOD_GSK3_1 | 65 | 72 | PF00069 | 0.474 |
MOD_GSK3_1 | 81 | 88 | PF00069 | 0.313 |
MOD_N-GLC_1 | 107 | 112 | PF02516 | 0.417 |
MOD_N-GLC_1 | 190 | 195 | PF02516 | 0.224 |
MOD_N-GLC_1 | 68 | 73 | PF02516 | 0.439 |
MOD_NEK2_1 | 233 | 238 | PF00069 | 0.403 |
MOD_NEK2_1 | 28 | 33 | PF00069 | 0.370 |
MOD_NEK2_1 | 319 | 324 | PF00069 | 0.481 |
MOD_NEK2_1 | 98 | 103 | PF00069 | 0.571 |
MOD_NEK2_2 | 36 | 41 | PF00069 | 0.387 |
MOD_PKA_1 | 147 | 153 | PF00069 | 0.599 |
MOD_PKA_2 | 147 | 153 | PF00069 | 0.552 |
MOD_PKA_2 | 168 | 174 | PF00069 | 0.495 |
MOD_PKA_2 | 233 | 239 | PF00069 | 0.409 |
MOD_PKA_2 | 330 | 336 | PF00069 | 0.361 |
MOD_PKA_2 | 352 | 358 | PF00069 | 0.547 |
MOD_PKA_2 | 8 | 14 | PF00069 | 0.356 |
MOD_PKA_2 | 98 | 104 | PF00069 | 0.620 |
MOD_PKB_1 | 145 | 153 | PF00069 | 0.586 |
MOD_Plk_1 | 107 | 113 | PF00069 | 0.416 |
MOD_Plk_1 | 320 | 326 | PF00069 | 0.468 |
MOD_Plk_1 | 386 | 392 | PF00069 | 0.379 |
MOD_Plk_4 | 320 | 326 | PF00069 | 0.344 |
MOD_Plk_4 | 330 | 336 | PF00069 | 0.559 |
MOD_Plk_4 | 53 | 59 | PF00069 | 0.460 |
MOD_Plk_4 | 90 | 96 | PF00069 | 0.365 |
MOD_Plk_4 | 98 | 104 | PF00069 | 0.449 |
MOD_ProDKin_1 | 169 | 175 | PF00069 | 0.502 |
MOD_ProDKin_1 | 274 | 280 | PF00069 | 0.524 |
MOD_ProDKin_1 | 303 | 309 | PF00069 | 0.412 |
MOD_ProDKin_1 | 375 | 381 | PF00069 | 0.616 |
MOD_SUMO_rev_2 | 19 | 26 | PF00179 | 0.362 |
TRG_DiLeu_BaEn_1 | 388 | 393 | PF01217 | 0.316 |
TRG_ENDOCYTIC_2 | 269 | 272 | PF00928 | 0.458 |
TRG_ENDOCYTIC_2 | 30 | 33 | PF00928 | 0.292 |
TRG_ER_diArg_1 | 145 | 148 | PF00400 | 0.559 |
TRG_ER_diArg_1 | 245 | 247 | PF00400 | 0.473 |
TRG_ER_diArg_1 | 310 | 312 | PF00400 | 0.481 |
TRG_NES_CRM1_1 | 92 | 105 | PF08389 | 0.364 |
TRG_NLS_MonoExtC_3 | 143 | 148 | PF00514 | 0.524 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5G8 | Leptomonas seymouri | 66% | 100% |
A0A1X0P342 | Trypanosomatidae | 40% | 100% |
A0A3Q8IFZ1 | Leishmania donovani | 100% | 100% |
A4HII8 | Leishmania braziliensis | 84% | 100% |
C9ZR53 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 91% |
E9B127 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
Q4Q738 | Leishmania major | 96% | 100% |
V5BMX2 | Trypanosoma cruzi | 42% | 100% |