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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4I3P2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 120 | 124 | PF00656 | 0.355 |
CLV_C14_Caspase3-7 | 389 | 393 | PF00656 | 0.501 |
CLV_NRD_NRD_1 | 295 | 297 | PF00675 | 0.456 |
CLV_NRD_NRD_1 | 365 | 367 | PF00675 | 0.441 |
CLV_NRD_NRD_1 | 385 | 387 | PF00675 | 0.321 |
CLV_NRD_NRD_1 | 458 | 460 | PF00675 | 0.595 |
CLV_PCSK_KEX2_1 | 295 | 297 | PF00082 | 0.433 |
CLV_PCSK_KEX2_1 | 365 | 367 | PF00082 | 0.441 |
CLV_PCSK_KEX2_1 | 457 | 459 | PF00082 | 0.423 |
CLV_PCSK_SKI1_1 | 33 | 37 | PF00082 | 0.421 |
CLV_PCSK_SKI1_1 | 458 | 462 | PF00082 | 0.424 |
CLV_Separin_Metazoa | 383 | 387 | PF03568 | 0.398 |
DEG_APCC_DBOX_1 | 32 | 40 | PF00400 | 0.371 |
DEG_SPOP_SBC_1 | 66 | 70 | PF00917 | 0.306 |
DOC_CYCLIN_RxL_1 | 435 | 445 | PF00134 | 0.388 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 141 | 150 | PF00134 | 0.405 |
DOC_MAPK_gen_1 | 365 | 373 | PF00069 | 0.414 |
DOC_PP2B_LxvP_1 | 236 | 239 | PF13499 | 0.407 |
DOC_PP2B_LxvP_1 | 320 | 323 | PF13499 | 0.482 |
DOC_PP4_FxxP_1 | 388 | 391 | PF00568 | 0.469 |
DOC_USP7_MATH_1 | 202 | 206 | PF00917 | 0.544 |
DOC_USP7_MATH_1 | 212 | 216 | PF00917 | 0.615 |
DOC_USP7_MATH_1 | 230 | 234 | PF00917 | 0.421 |
DOC_USP7_MATH_1 | 274 | 278 | PF00917 | 0.638 |
DOC_USP7_MATH_1 | 66 | 70 | PF00917 | 0.375 |
DOC_USP7_MATH_2 | 65 | 71 | PF00917 | 0.282 |
DOC_WW_Pin1_4 | 221 | 226 | PF00397 | 0.550 |
DOC_WW_Pin1_4 | 313 | 318 | PF00397 | 0.547 |
DOC_WW_Pin1_4 | 387 | 392 | PF00397 | 0.479 |
DOC_WW_Pin1_4 | 418 | 423 | PF00397 | 0.413 |
DOC_WW_Pin1_4 | 60 | 65 | PF00397 | 0.396 |
LIG_14-3-3_CanoR_1 | 153 | 161 | PF00244 | 0.365 |
LIG_14-3-3_CanoR_1 | 261 | 271 | PF00244 | 0.517 |
LIG_14-3-3_CanoR_1 | 313 | 317 | PF00244 | 0.668 |
LIG_14-3-3_CanoR_1 | 386 | 391 | PF00244 | 0.417 |
LIG_14-3-3_CterR_2 | 458 | 463 | PF00244 | 0.426 |
LIG_Actin_WH2_2 | 139 | 155 | PF00022 | 0.485 |
LIG_APCC_ABBA_1 | 168 | 173 | PF00400 | 0.439 |
LIG_BRCT_BRCA1_1 | 111 | 115 | PF00533 | 0.279 |
LIG_CaM_NSCaTE_8 | 351 | 358 | PF13499 | 0.343 |
LIG_CSL_BTD_1 | 222 | 225 | PF09270 | 0.611 |
LIG_deltaCOP1_diTrp_1 | 349 | 353 | PF00928 | 0.309 |
LIG_FHA_1 | 146 | 152 | PF00498 | 0.386 |
LIG_FHA_1 | 239 | 245 | PF00498 | 0.427 |
LIG_FHA_1 | 263 | 269 | PF00498 | 0.510 |
LIG_FHA_1 | 313 | 319 | PF00498 | 0.599 |
LIG_FHA_1 | 343 | 349 | PF00498 | 0.542 |
LIG_FHA_1 | 4 | 10 | PF00498 | 0.582 |
LIG_FHA_2 | 21 | 27 | PF00498 | 0.361 |
LIG_FHA_2 | 250 | 256 | PF00498 | 0.448 |
LIG_FHA_2 | 5 | 11 | PF00498 | 0.669 |
LIG_LIR_Gen_1 | 112 | 121 | PF02991 | 0.279 |
LIG_LIR_Gen_1 | 6 | 15 | PF02991 | 0.558 |
LIG_LIR_Gen_1 | 86 | 94 | PF02991 | 0.301 |
LIG_LIR_Nem_3 | 396 | 401 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 434 | 440 | PF02991 | 0.389 |
LIG_LIR_Nem_3 | 86 | 90 | PF02991 | 0.301 |
LIG_NRBOX | 369 | 375 | PF00104 | 0.390 |
LIG_PDZ_Class_1 | 458 | 463 | PF00595 | 0.426 |
LIG_PTB_Apo_2 | 2 | 9 | PF02174 | 0.537 |
LIG_SH2_CRK | 425 | 429 | PF00017 | 0.495 |
LIG_SH2_STAT5 | 128 | 131 | PF00017 | 0.350 |
LIG_SH2_STAT5 | 191 | 194 | PF00017 | 0.498 |
LIG_SH2_STAT5 | 407 | 410 | PF00017 | 0.376 |
LIG_SH2_STAT5 | 48 | 51 | PF00017 | 0.343 |
LIG_SH3_3 | 21 | 27 | PF00018 | 0.420 |
LIG_SH3_3 | 268 | 274 | PF00018 | 0.528 |
LIG_SH3_3 | 328 | 334 | PF00018 | 0.504 |
LIG_SH3_3 | 59 | 65 | PF00018 | 0.355 |
LIG_SUMO_SIM_par_1 | 16 | 23 | PF11976 | 0.498 |
LIG_SUMO_SIM_par_1 | 315 | 321 | PF11976 | 0.568 |
LIG_SUMO_SIM_par_1 | 369 | 375 | PF11976 | 0.392 |
LIG_UBA3_1 | 126 | 134 | PF00899 | 0.445 |
LIG_UBA3_1 | 90 | 97 | PF00899 | 0.391 |
MOD_CDK_SPxK_1 | 418 | 424 | PF00069 | 0.433 |
MOD_CK1_1 | 13 | 19 | PF00069 | 0.522 |
MOD_CK1_1 | 205 | 211 | PF00069 | 0.566 |
MOD_CK1_1 | 215 | 221 | PF00069 | 0.511 |
MOD_CK1_1 | 266 | 272 | PF00069 | 0.501 |
MOD_CK1_1 | 329 | 335 | PF00069 | 0.700 |
MOD_CK1_1 | 4 | 10 | PF00069 | 0.627 |
MOD_CK1_1 | 68 | 74 | PF00069 | 0.417 |
MOD_CK2_1 | 26 | 32 | PF00069 | 0.330 |
MOD_CK2_1 | 266 | 272 | PF00069 | 0.548 |
MOD_CK2_1 | 4 | 10 | PF00069 | 0.536 |
MOD_Cter_Amidation | 293 | 296 | PF01082 | 0.491 |
MOD_GlcNHglycan | 129 | 132 | PF01048 | 0.410 |
MOD_GlcNHglycan | 13 | 16 | PF01048 | 0.658 |
MOD_GlcNHglycan | 172 | 177 | PF01048 | 0.545 |
MOD_GlcNHglycan | 232 | 235 | PF01048 | 0.601 |
MOD_GlcNHglycan | 268 | 271 | PF01048 | 0.446 |
MOD_GlcNHglycan | 276 | 279 | PF01048 | 0.540 |
MOD_GlcNHglycan | 330 | 334 | PF01048 | 0.700 |
MOD_GlcNHglycan | 425 | 428 | PF01048 | 0.613 |
MOD_GlcNHglycan | 94 | 97 | PF01048 | 0.330 |
MOD_GSK3_1 | 101 | 108 | PF00069 | 0.289 |
MOD_GSK3_1 | 137 | 144 | PF00069 | 0.492 |
MOD_GSK3_1 | 230 | 237 | PF00069 | 0.525 |
MOD_GSK3_1 | 262 | 269 | PF00069 | 0.540 |
MOD_GSK3_1 | 274 | 281 | PF00069 | 0.536 |
MOD_GSK3_1 | 442 | 449 | PF00069 | 0.559 |
MOD_GSK3_1 | 9 | 16 | PF00069 | 0.550 |
MOD_N-GLC_1 | 4 | 9 | PF02516 | 0.596 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.556 |
MOD_NEK2_1 | 111 | 116 | PF00069 | 0.342 |
MOD_NEK2_1 | 127 | 132 | PF00069 | 0.313 |
MOD_NEK2_1 | 141 | 146 | PF00069 | 0.467 |
MOD_NEK2_1 | 152 | 157 | PF00069 | 0.500 |
MOD_NEK2_1 | 183 | 188 | PF00069 | 0.442 |
MOD_NEK2_1 | 249 | 254 | PF00069 | 0.411 |
MOD_NEK2_1 | 262 | 267 | PF00069 | 0.418 |
MOD_NEK2_1 | 374 | 379 | PF00069 | 0.358 |
MOD_NEK2_1 | 423 | 428 | PF00069 | 0.560 |
MOD_NEK2_1 | 442 | 447 | PF00069 | 0.421 |
MOD_NEK2_1 | 9 | 14 | PF00069 | 0.544 |
MOD_PIKK_1 | 263 | 269 | PF00454 | 0.461 |
MOD_PIKK_1 | 442 | 448 | PF00454 | 0.402 |
MOD_PKA_1 | 386 | 392 | PF00069 | 0.460 |
MOD_PKA_2 | 152 | 158 | PF00069 | 0.409 |
MOD_PKA_2 | 263 | 269 | PF00069 | 0.528 |
MOD_PKA_2 | 312 | 318 | PF00069 | 0.411 |
MOD_PKA_2 | 423 | 429 | PF00069 | 0.506 |
MOD_Plk_1 | 20 | 26 | PF00069 | 0.338 |
MOD_Plk_1 | 202 | 208 | PF00069 | 0.491 |
MOD_Plk_1 | 4 | 10 | PF00069 | 0.536 |
MOD_Plk_4 | 111 | 117 | PF00069 | 0.435 |
MOD_Plk_4 | 183 | 189 | PF00069 | 0.444 |
MOD_Plk_4 | 249 | 255 | PF00069 | 0.449 |
MOD_Plk_4 | 369 | 375 | PF00069 | 0.421 |
MOD_Plk_4 | 4 | 10 | PF00069 | 0.649 |
MOD_ProDKin_1 | 221 | 227 | PF00069 | 0.547 |
MOD_ProDKin_1 | 313 | 319 | PF00069 | 0.541 |
MOD_ProDKin_1 | 387 | 393 | PF00069 | 0.490 |
MOD_ProDKin_1 | 418 | 424 | PF00069 | 0.422 |
MOD_ProDKin_1 | 60 | 66 | PF00069 | 0.396 |
MOD_SUMO_rev_2 | 392 | 401 | PF00179 | 0.425 |
TRG_DiLeu_BaLyEn_6 | 48 | 53 | PF01217 | 0.453 |
TRG_ER_diArg_1 | 295 | 297 | PF00400 | 0.433 |
TRG_ER_diArg_1 | 456 | 459 | PF00400 | 0.421 |
TRG_ER_diArg_1 | 78 | 81 | PF00400 | 0.362 |
TRG_Pf-PMV_PEXEL_1 | 55 | 59 | PF00026 | 0.334 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I7G4 | Leptomonas seymouri | 47% | 71% |
A0A1X0NQX3 | Trypanosomatidae | 30% | 67% |
A0A3Q8IDU2 | Leishmania donovani | 100% | 74% |
A0A3S5ISD3 | Trypanosoma rangeli | 29% | 74% |
A4HGL7 | Leishmania braziliensis | 75% | 100% |
D0A8C2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 83% |
E9AZY3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
Q4Q8A2 | Leishmania major | 93% | 100% |
V5DBC6 | Trypanosoma cruzi | 32% | 90% |