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: 11 |
NetGPI | no | yes: 0, no: 11 |
Related structures:
AlphaFold database: A4IE48
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 225 | 229 | PF00656 | 0.533 |
CLV_C14_Caspase3-7 | 9 | 13 | PF00656 | 0.486 |
CLV_NRD_NRD_1 | 124 | 126 | PF00675 | 0.434 |
CLV_NRD_NRD_1 | 197 | 199 | PF00675 | 0.495 |
CLV_NRD_NRD_1 | 309 | 311 | PF00675 | 0.409 |
CLV_NRD_NRD_1 | 332 | 334 | PF00675 | 0.380 |
CLV_NRD_NRD_1 | 339 | 341 | PF00675 | 0.353 |
CLV_NRD_NRD_1 | 355 | 357 | PF00675 | 0.398 |
CLV_NRD_NRD_1 | 405 | 407 | PF00675 | 0.541 |
CLV_NRD_NRD_1 | 90 | 92 | PF00675 | 0.655 |
CLV_PCSK_KEX2_1 | 124 | 126 | PF00082 | 0.466 |
CLV_PCSK_KEX2_1 | 197 | 199 | PF00082 | 0.495 |
CLV_PCSK_KEX2_1 | 309 | 311 | PF00082 | 0.424 |
CLV_PCSK_KEX2_1 | 332 | 334 | PF00082 | 0.419 |
CLV_PCSK_KEX2_1 | 35 | 37 | PF00082 | 0.686 |
CLV_PCSK_KEX2_1 | 355 | 357 | PF00082 | 0.398 |
CLV_PCSK_KEX2_1 | 405 | 407 | PF00082 | 0.542 |
CLV_PCSK_KEX2_1 | 90 | 92 | PF00082 | 0.607 |
CLV_PCSK_PC1ET2_1 | 35 | 37 | PF00082 | 0.664 |
CLV_PCSK_SKI1_1 | 127 | 131 | PF00082 | 0.435 |
CLV_PCSK_SKI1_1 | 187 | 191 | PF00082 | 0.431 |
CLV_PCSK_SKI1_1 | 197 | 201 | PF00082 | 0.455 |
CLV_PCSK_SKI1_1 | 260 | 264 | PF00082 | 0.403 |
DEG_APCC_DBOX_1 | 126 | 134 | PF00400 | 0.412 |
DEG_MDM2_SWIB_1 | 211 | 219 | PF02201 | 0.357 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.566 |
DOC_CKS1_1 | 22 | 27 | PF01111 | 0.575 |
DOC_CYCLIN_RxL_1 | 172 | 183 | PF00134 | 0.391 |
DOC_CYCLIN_RxL_1 | 254 | 265 | PF00134 | 0.430 |
DOC_MAPK_gen_1 | 124 | 130 | PF00069 | 0.525 |
DOC_MAPK_gen_1 | 338 | 348 | PF00069 | 0.398 |
DOC_MAPK_gen_1 | 366 | 374 | PF00069 | 0.424 |
DOC_MAPK_MEF2A_6 | 340 | 348 | PF00069 | 0.389 |
DOC_USP7_MATH_1 | 11 | 15 | PF00917 | 0.678 |
DOC_USP7_MATH_1 | 129 | 133 | PF00917 | 0.460 |
DOC_USP7_MATH_1 | 302 | 306 | PF00917 | 0.454 |
DOC_USP7_MATH_1 | 354 | 358 | PF00917 | 0.411 |
DOC_USP7_MATH_1 | 421 | 425 | PF00917 | 0.642 |
DOC_USP7_MATH_1 | 60 | 64 | PF00917 | 0.744 |
DOC_WW_Pin1_4 | 21 | 26 | PF00397 | 0.693 |
LIG_14-3-3_CanoR_1 | 187 | 194 | PF00244 | 0.507 |
LIG_14-3-3_CanoR_1 | 21 | 25 | PF00244 | 0.746 |
LIG_14-3-3_CanoR_1 | 257 | 263 | PF00244 | 0.452 |
LIG_14-3-3_CanoR_1 | 303 | 307 | PF00244 | 0.443 |
LIG_14-3-3_CanoR_1 | 355 | 359 | PF00244 | 0.535 |
LIG_14-3-3_CanoR_1 | 412 | 418 | PF00244 | 0.655 |
LIG_14-3-3_CanoR_1 | 65 | 75 | PF00244 | 0.495 |
LIG_Actin_WH2_2 | 241 | 259 | PF00022 | 0.428 |
LIG_Actin_WH2_2 | 396 | 414 | PF00022 | 0.454 |
LIG_AP_GAE_1 | 116 | 122 | PF02883 | 0.575 |
LIG_BRCT_BRCA1_1 | 395 | 399 | PF00533 | 0.496 |
LIG_eIF4E_1 | 164 | 170 | PF01652 | 0.376 |
LIG_FHA_1 | 2 | 8 | PF00498 | 0.617 |
LIG_FHA_1 | 25 | 31 | PF00498 | 0.570 |
LIG_FHA_1 | 367 | 373 | PF00498 | 0.400 |
LIG_FHA_1 | 385 | 391 | PF00498 | 0.480 |
LIG_FHA_2 | 133 | 139 | PF00498 | 0.625 |
LIG_FHA_2 | 154 | 160 | PF00498 | 0.495 |
LIG_FHA_2 | 325 | 331 | PF00498 | 0.470 |
LIG_FHA_2 | 7 | 13 | PF00498 | 0.481 |
LIG_Integrin_RGD_1 | 85 | 87 | PF01839 | 0.665 |
LIG_LIR_Gen_1 | 116 | 126 | PF02991 | 0.421 |
LIG_LIR_Nem_3 | 116 | 122 | PF02991 | 0.434 |
LIG_LIR_Nem_3 | 207 | 211 | PF02991 | 0.381 |
LIG_NRBOX | 343 | 349 | PF00104 | 0.388 |
LIG_Pex14_2 | 211 | 215 | PF04695 | 0.351 |
LIG_SH2_CRK | 34 | 38 | PF00017 | 0.485 |
LIG_SH2_GRB2like | 351 | 354 | PF00017 | 0.386 |
LIG_SH2_SRC | 351 | 354 | PF00017 | 0.405 |
LIG_SH2_STAP1 | 258 | 262 | PF00017 | 0.433 |
LIG_SH2_STAP1 | 409 | 413 | PF00017 | 0.505 |
LIG_SH2_STAT3 | 168 | 171 | PF00017 | 0.510 |
LIG_SH2_STAT3 | 339 | 342 | PF00017 | 0.499 |
LIG_SH2_STAT5 | 168 | 171 | PF00017 | 0.398 |
LIG_SH2_STAT5 | 278 | 281 | PF00017 | 0.549 |
LIG_SH2_STAT5 | 335 | 338 | PF00017 | 0.510 |
LIG_SH2_STAT5 | 351 | 354 | PF00017 | 0.412 |
LIG_SH3_3 | 104 | 110 | PF00018 | 0.682 |
LIG_SH3_3 | 19 | 25 | PF00018 | 0.588 |
LIG_SH3_3 | 27 | 33 | PF00018 | 0.572 |
LIG_SUMO_SIM_anti_2 | 146 | 153 | PF11976 | 0.513 |
LIG_SUMO_SIM_anti_2 | 230 | 235 | PF11976 | 0.515 |
LIG_SUMO_SIM_anti_2 | 343 | 348 | PF11976 | 0.383 |
LIG_TRAF2_1 | 221 | 224 | PF00917 | 0.426 |
MOD_CK1_1 | 102 | 108 | PF00069 | 0.714 |
MOD_CK1_1 | 132 | 138 | PF00069 | 0.499 |
MOD_CK1_1 | 153 | 159 | PF00069 | 0.491 |
MOD_CK1_1 | 20 | 26 | PF00069 | 0.715 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.697 |
MOD_CK1_1 | 357 | 363 | PF00069 | 0.529 |
MOD_CK1_1 | 393 | 399 | PF00069 | 0.538 |
MOD_CK1_1 | 54 | 60 | PF00069 | 0.768 |
MOD_CK1_1 | 63 | 69 | PF00069 | 0.644 |
MOD_CK2_1 | 132 | 138 | PF00069 | 0.530 |
MOD_CK2_1 | 153 | 159 | PF00069 | 0.484 |
MOD_CK2_1 | 258 | 264 | PF00069 | 0.497 |
MOD_CK2_1 | 302 | 308 | PF00069 | 0.451 |
MOD_CK2_1 | 324 | 330 | PF00069 | 0.496 |
MOD_DYRK1A_RPxSP_1 | 21 | 25 | PF00069 | 0.490 |
MOD_GlcNHglycan | 383 | 387 | PF01048 | 0.495 |
MOD_GlcNHglycan | 392 | 395 | PF01048 | 0.531 |
MOD_GlcNHglycan | 421 | 424 | PF01048 | 0.764 |
MOD_GlcNHglycan | 56 | 59 | PF01048 | 0.729 |
MOD_GlcNHglycan | 66 | 69 | PF01048 | 0.650 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.718 |
MOD_GSK3_1 | 13 | 20 | PF00069 | 0.719 |
MOD_GSK3_1 | 258 | 265 | PF00069 | 0.453 |
MOD_GSK3_1 | 324 | 331 | PF00069 | 0.531 |
MOD_GSK3_1 | 60 | 67 | PF00069 | 0.660 |
MOD_LATS_1 | 185 | 191 | PF00433 | 0.428 |
MOD_N-GLC_1 | 1 | 6 | PF02516 | 0.558 |
MOD_N-GLC_1 | 366 | 371 | PF02516 | 0.495 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.589 |
MOD_NEK2_1 | 211 | 216 | PF00069 | 0.497 |
MOD_NEK2_1 | 256 | 261 | PF00069 | 0.507 |
MOD_NEK2_1 | 262 | 267 | PF00069 | 0.431 |
MOD_NEK2_1 | 390 | 395 | PF00069 | 0.518 |
MOD_NEK2_1 | 411 | 416 | PF00069 | 0.515 |
MOD_NEK2_1 | 71 | 76 | PF00069 | 0.688 |
MOD_NEK2_2 | 302 | 307 | PF00069 | 0.446 |
MOD_NEK2_2 | 421 | 426 | PF00069 | 0.562 |
MOD_NEK2_2 | 60 | 65 | PF00069 | 0.491 |
MOD_PIKK_1 | 357 | 363 | PF00454 | 0.467 |
MOD_PIKK_1 | 411 | 417 | PF00454 | 0.679 |
MOD_PIKK_1 | 46 | 52 | PF00454 | 0.732 |
MOD_PKA_2 | 20 | 26 | PF00069 | 0.740 |
MOD_PKA_2 | 256 | 262 | PF00069 | 0.506 |
MOD_PKA_2 | 302 | 308 | PF00069 | 0.451 |
MOD_PKA_2 | 354 | 360 | PF00069 | 0.528 |
MOD_PKA_2 | 411 | 417 | PF00069 | 0.651 |
MOD_PKA_2 | 64 | 70 | PF00069 | 0.514 |
MOD_Plk_1 | 11 | 17 | PF00069 | 0.506 |
MOD_Plk_4 | 26 | 32 | PF00069 | 0.718 |
MOD_Plk_4 | 302 | 308 | PF00069 | 0.451 |
MOD_Plk_4 | 368 | 374 | PF00069 | 0.415 |
MOD_Plk_4 | 398 | 404 | PF00069 | 0.666 |
MOD_ProDKin_1 | 21 | 27 | PF00069 | 0.696 |
TRG_DiLeu_BaEn_1 | 343 | 348 | PF01217 | 0.383 |
TRG_DiLeu_BaEn_4 | 195 | 201 | PF01217 | 0.503 |
TRG_DiLeu_BaLyEn_6 | 251 | 256 | PF01217 | 0.568 |
TRG_ER_diArg_1 | 124 | 127 | PF00400 | 0.500 |
TRG_ER_diArg_1 | 197 | 199 | PF00400 | 0.543 |
TRG_ER_diArg_1 | 332 | 334 | PF00400 | 0.398 |
TRG_Pf-PMV_PEXEL_1 | 175 | 180 | PF00026 | 0.397 |
TRG_Pf-PMV_PEXEL_1 | 187 | 191 | PF00026 | 0.434 |
TRG_Pf-PMV_PEXEL_1 | 197 | 201 | PF00026 | 0.492 |
TRG_Pf-PMV_PEXEL_1 | 260 | 264 | PF00026 | 0.391 |
TRG_Pf-PMV_PEXEL_1 | 332 | 337 | PF00026 | 0.428 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7J8 | Leptomonas seymouri | 65% | 100% |
A0A0S4JG62 | Bodo saltans | 51% | 100% |
A0A1X0P1T1 | Trypanosomatidae | 54% | 100% |
A0A3Q8ILB9 | Leishmania donovani | 100% | 100% |
A0A422P583 | Trypanosoma rangeli | 56% | 100% |
A4HPU5 | Leishmania braziliensis | 79% | 100% |
D0A491 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 50% | 100% |
E9ATL0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
Q4Q0Y8 | Leishmania major | 94% | 100% |
V5BQ98 | Trypanosoma cruzi | 57% | 100% |