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: 7 |
NetGPI | no | yes: 0, no: 7 |
Related structures:
AlphaFold database: A4I7Z1
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 434 | 438 | PF00656 | 0.717 |
CLV_NRD_NRD_1 | 205 | 207 | PF00675 | 0.612 |
CLV_NRD_NRD_1 | 295 | 297 | PF00675 | 0.431 |
CLV_NRD_NRD_1 | 348 | 350 | PF00675 | 0.524 |
CLV_NRD_NRD_1 | 362 | 364 | PF00675 | 0.647 |
CLV_NRD_NRD_1 | 400 | 402 | PF00675 | 0.590 |
CLV_PCSK_FUR_1 | 349 | 353 | PF00082 | 0.553 |
CLV_PCSK_KEX2_1 | 118 | 120 | PF00082 | 0.519 |
CLV_PCSK_KEX2_1 | 205 | 207 | PF00082 | 0.612 |
CLV_PCSK_KEX2_1 | 295 | 297 | PF00082 | 0.499 |
CLV_PCSK_KEX2_1 | 351 | 353 | PF00082 | 0.578 |
CLV_PCSK_KEX2_1 | 362 | 364 | PF00082 | 0.667 |
CLV_PCSK_KEX2_1 | 488 | 490 | PF00082 | 0.510 |
CLV_PCSK_PC1ET2_1 | 118 | 120 | PF00082 | 0.451 |
CLV_PCSK_PC1ET2_1 | 351 | 353 | PF00082 | 0.578 |
CLV_PCSK_PC1ET2_1 | 488 | 490 | PF00082 | 0.510 |
CLV_PCSK_PC7_1 | 114 | 120 | PF00082 | 0.506 |
CLV_PCSK_PC7_1 | 347 | 353 | PF00082 | 0.550 |
CLV_PCSK_SKI1_1 | 217 | 221 | PF00082 | 0.637 |
CLV_PCSK_SKI1_1 | 23 | 27 | PF00082 | 0.614 |
CLV_PCSK_SKI1_1 | 368 | 372 | PF00082 | 0.530 |
CLV_PCSK_SKI1_1 | 468 | 472 | PF00082 | 0.548 |
DEG_APCC_DBOX_1 | 233 | 241 | PF00400 | 0.650 |
DEG_APCC_KENBOX_2 | 180 | 184 | PF00400 | 0.479 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.566 |
DEG_SPOP_SBC_1 | 428 | 432 | PF00917 | 0.631 |
DOC_ANK_TNKS_1 | 332 | 339 | PF00023 | 0.500 |
DOC_MAPK_gen_1 | 293 | 300 | PF00069 | 0.385 |
DOC_MAPK_gen_1 | 301 | 309 | PF00069 | 0.364 |
DOC_MAPK_MEF2A_6 | 142 | 151 | PF00069 | 0.408 |
DOC_USP7_MATH_1 | 221 | 225 | PF00917 | 0.609 |
DOC_USP7_MATH_1 | 230 | 234 | PF00917 | 0.577 |
DOC_USP7_MATH_1 | 24 | 28 | PF00917 | 0.630 |
DOC_USP7_MATH_1 | 397 | 401 | PF00917 | 0.661 |
DOC_USP7_MATH_1 | 428 | 432 | PF00917 | 0.664 |
DOC_USP7_UBL2_3 | 128 | 132 | PF12436 | 0.424 |
DOC_USP7_UBL2_3 | 367 | 371 | PF12436 | 0.644 |
DOC_WW_Pin1_4 | 11 | 16 | PF00397 | 0.619 |
DOC_WW_Pin1_4 | 191 | 196 | PF00397 | 0.479 |
DOC_WW_Pin1_4 | 25 | 30 | PF00397 | 0.621 |
DOC_WW_Pin1_4 | 424 | 429 | PF00397 | 0.676 |
DOC_WW_Pin1_4 | 437 | 442 | PF00397 | 0.593 |
LIG_14-3-3_CanoR_1 | 23 | 29 | PF00244 | 0.555 |
LIG_14-3-3_CanoR_1 | 401 | 410 | PF00244 | 0.588 |
LIG_APCC_ABBA_1 | 136 | 141 | PF00400 | 0.432 |
LIG_BRCT_BRCA1_1 | 27 | 31 | PF00533 | 0.618 |
LIG_Clathr_ClatBox_1 | 146 | 150 | PF01394 | 0.468 |
LIG_EH1_1 | 30 | 38 | PF00400 | 0.574 |
LIG_FHA_1 | 270 | 276 | PF00498 | 0.623 |
LIG_FHA_1 | 469 | 475 | PF00498 | 0.546 |
LIG_FHA_1 | 87 | 93 | PF00498 | 0.419 |
LIG_FHA_2 | 259 | 265 | PF00498 | 0.622 |
LIG_FHA_2 | 330 | 336 | PF00498 | 0.406 |
LIG_FHA_2 | 432 | 438 | PF00498 | 0.723 |
LIG_FHA_2 | 450 | 456 | PF00498 | 0.738 |
LIG_FHA_2 | 473 | 479 | PF00498 | 0.524 |
LIG_LIR_Gen_1 | 150 | 159 | PF02991 | 0.525 |
LIG_LIR_Gen_1 | 294 | 305 | PF02991 | 0.455 |
LIG_LIR_Gen_1 | 463 | 474 | PF02991 | 0.565 |
LIG_LIR_Gen_1 | 54 | 64 | PF02991 | 0.494 |
LIG_LIR_Gen_1 | 85 | 96 | PF02991 | 0.473 |
LIG_LIR_Nem_3 | 150 | 154 | PF02991 | 0.538 |
LIG_LIR_Nem_3 | 294 | 300 | PF02991 | 0.455 |
LIG_LIR_Nem_3 | 437 | 442 | PF02991 | 0.587 |
LIG_LIR_Nem_3 | 463 | 469 | PF02991 | 0.619 |
LIG_LIR_Nem_3 | 54 | 60 | PF02991 | 0.504 |
LIG_LIR_Nem_3 | 85 | 91 | PF02991 | 0.474 |
LIG_NRBOX | 236 | 242 | PF00104 | 0.596 |
LIG_Pex14_2 | 57 | 61 | PF04695 | 0.494 |
LIG_REV1ctd_RIR_1 | 58 | 66 | PF16727 | 0.461 |
LIG_SH2_PTP2 | 297 | 300 | PF00017 | 0.367 |
LIG_SH2_STAT3 | 236 | 239 | PF00017 | 0.538 |
LIG_SH2_STAT3 | 340 | 343 | PF00017 | 0.527 |
LIG_SH2_STAT5 | 236 | 239 | PF00017 | 0.522 |
LIG_SH2_STAT5 | 297 | 300 | PF00017 | 0.571 |
LIG_SH2_STAT5 | 466 | 469 | PF00017 | 0.549 |
LIG_SH3_1 | 26 | 32 | PF00018 | 0.548 |
LIG_SH3_2 | 29 | 34 | PF14604 | 0.566 |
LIG_SH3_3 | 26 | 32 | PF00018 | 0.567 |
LIG_Sin3_3 | 109 | 116 | PF02671 | 0.514 |
LIG_SUMO_SIM_par_1 | 145 | 150 | PF11976 | 0.422 |
LIG_SUMO_SIM_par_1 | 255 | 261 | PF11976 | 0.579 |
LIG_SUMO_SIM_par_1 | 305 | 311 | PF11976 | 0.393 |
LIG_TRAF2_1 | 341 | 344 | PF00917 | 0.647 |
LIG_TRAF2_1 | 403 | 406 | PF00917 | 0.689 |
LIG_TRAF2_1 | 71 | 74 | PF00917 | 0.528 |
LIG_TRAF2_1 | 82 | 85 | PF00917 | 0.399 |
LIG_TYR_ITIM | 464 | 469 | PF00017 | 0.479 |
LIG_UBA3_1 | 126 | 132 | PF00899 | 0.498 |
MOD_CK1_1 | 199 | 205 | PF00069 | 0.605 |
MOD_CK1_1 | 244 | 250 | PF00069 | 0.673 |
MOD_CK1_1 | 400 | 406 | PF00069 | 0.664 |
MOD_CK1_1 | 427 | 433 | PF00069 | 0.635 |
MOD_CK1_1 | 440 | 446 | PF00069 | 0.606 |
MOD_CK2_1 | 191 | 197 | PF00069 | 0.488 |
MOD_CK2_1 | 329 | 335 | PF00069 | 0.407 |
MOD_CK2_1 | 400 | 406 | PF00069 | 0.843 |
MOD_CK2_1 | 449 | 455 | PF00069 | 0.724 |
MOD_CK2_1 | 472 | 478 | PF00069 | 0.473 |
MOD_CK2_1 | 68 | 74 | PF00069 | 0.485 |
MOD_GlcNHglycan | 353 | 357 | PF01048 | 0.499 |
MOD_GlcNHglycan | 442 | 445 | PF01048 | 0.706 |
MOD_GlcNHglycan | 483 | 486 | PF01048 | 0.513 |
MOD_GlcNHglycan | 70 | 73 | PF01048 | 0.458 |
MOD_GlcNHglycan | 8 | 11 | PF01048 | 0.606 |
MOD_GSK3_1 | 221 | 228 | PF00069 | 0.702 |
MOD_GSK3_1 | 243 | 250 | PF00069 | 0.547 |
MOD_GSK3_1 | 269 | 276 | PF00069 | 0.557 |
MOD_GSK3_1 | 397 | 404 | PF00069 | 0.766 |
MOD_GSK3_1 | 424 | 431 | PF00069 | 0.640 |
MOD_GSK3_1 | 468 | 475 | PF00069 | 0.558 |
MOD_N-GLC_1 | 437 | 442 | PF02516 | 0.636 |
MOD_NEK2_1 | 213 | 218 | PF00069 | 0.709 |
MOD_NEK2_1 | 241 | 246 | PF00069 | 0.541 |
MOD_NEK2_1 | 269 | 274 | PF00069 | 0.674 |
MOD_NEK2_1 | 329 | 334 | PF00069 | 0.469 |
MOD_PKA_1 | 205 | 211 | PF00069 | 0.615 |
MOD_PKA_1 | 401 | 407 | PF00069 | 0.599 |
MOD_PKA_2 | 199 | 205 | PF00069 | 0.606 |
MOD_PKA_2 | 225 | 231 | PF00069 | 0.566 |
MOD_PKA_2 | 400 | 406 | PF00069 | 0.687 |
MOD_Plk_1 | 196 | 202 | PF00069 | 0.573 |
MOD_ProDKin_1 | 11 | 17 | PF00069 | 0.620 |
MOD_ProDKin_1 | 191 | 197 | PF00069 | 0.481 |
MOD_ProDKin_1 | 25 | 31 | PF00069 | 0.615 |
MOD_ProDKin_1 | 424 | 430 | PF00069 | 0.676 |
MOD_ProDKin_1 | 437 | 443 | PF00069 | 0.594 |
MOD_SUMO_for_1 | 487 | 490 | PF00179 | 0.456 |
TRG_DiLeu_BaEn_1 | 107 | 112 | PF01217 | 0.563 |
TRG_DiLeu_BaEn_1 | 150 | 155 | PF01217 | 0.480 |
TRG_DiLeu_BaEn_3 | 121 | 127 | PF01217 | 0.404 |
TRG_DiLeu_BaLyEn_6 | 264 | 269 | PF01217 | 0.604 |
TRG_DiLeu_BaLyEn_6 | 370 | 375 | PF01217 | 0.514 |
TRG_ENDOCYTIC_2 | 297 | 300 | PF00928 | 0.451 |
TRG_ENDOCYTIC_2 | 466 | 469 | PF00928 | 0.721 |
TRG_ER_diArg_1 | 286 | 289 | PF00400 | 0.503 |
TRG_ER_diArg_1 | 295 | 297 | PF00400 | 0.494 |
TRG_ER_diArg_1 | 375 | 378 | PF00400 | 0.626 |
TRG_NES_CRM1_1 | 124 | 140 | PF08389 | 0.446 |
TRG_Pf-PMV_PEXEL_1 | 164 | 168 | PF00026 | 0.503 |
TRG_Pf-PMV_PEXEL_1 | 373 | 377 | PF00026 | 0.516 |
TRG_Pf-PMV_PEXEL_1 | 380 | 384 | PF00026 | 0.575 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IMW1 | Leptomonas seymouri | 41% | 85% |
A0A3Q8IG72 | Leishmania donovani | 99% | 100% |
A0A3R7MFC1 | Trypanosoma rangeli | 29% | 82% |
A4HKG3 | Leishmania braziliensis | 62% | 100% |
E9B2V2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |
Q4Q5A4 | Leishmania major | 86% | 100% |