Membrane associated proteins, Flavo subunit-like
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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 7 |
NetGPI | no | yes: 0, no: 7 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pescher et al. (upgregulation) | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Lahav et al. - mRNA
- Protein
|
Related structures:
AlphaFold database: A4HTA6
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 8 |
GO:0005488 | binding | 1 | 8 |
GO:0016491 | oxidoreductase activity | 2 | 8 |
GO:0020037 | heme binding | 4 | 6 |
GO:0043167 | ion binding | 2 | 8 |
GO:0043169 | cation binding | 3 | 6 |
GO:0046872 | metal ion binding | 4 | 6 |
GO:0046906 | tetrapyrrole binding | 3 | 6 |
GO:0097159 | organic cyclic compound binding | 2 | 8 |
GO:1901363 | heterocyclic compound binding | 2 | 8 |
GO:0000166 | nucleotide binding | 3 | 2 |
GO:0010181 | FMN binding | 4 | 2 |
GO:0032553 | ribonucleotide binding | 3 | 2 |
GO:0036094 | small molecule binding | 2 | 2 |
GO:0043168 | anion binding | 3 | 2 |
GO:0097367 | carbohydrate derivative binding | 2 | 2 |
GO:1901265 | nucleoside phosphate binding | 3 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 372 | 376 | PF00656 | 0.417 |
CLV_C14_Caspase3-7 | 481 | 485 | PF00656 | 0.598 |
CLV_NRD_NRD_1 | 208 | 210 | PF00675 | 0.369 |
CLV_PCSK_KEX2_1 | 208 | 210 | PF00082 | 0.405 |
CLV_PCSK_KEX2_1 | 251 | 253 | PF00082 | 0.420 |
CLV_PCSK_KEX2_1 | 299 | 301 | PF00082 | 0.450 |
CLV_PCSK_KEX2_1 | 312 | 314 | PF00082 | 0.381 |
CLV_PCSK_KEX2_1 | 491 | 493 | PF00082 | 0.583 |
CLV_PCSK_PC1ET2_1 | 251 | 253 | PF00082 | 0.420 |
CLV_PCSK_PC1ET2_1 | 299 | 301 | PF00082 | 0.433 |
CLV_PCSK_PC1ET2_1 | 312 | 314 | PF00082 | 0.287 |
CLV_PCSK_PC1ET2_1 | 491 | 493 | PF00082 | 0.583 |
CLV_PCSK_PC7_1 | 247 | 253 | PF00082 | 0.416 |
CLV_PCSK_SKI1_1 | 300 | 304 | PF00082 | 0.413 |
CLV_PCSK_SKI1_1 | 334 | 338 | PF00082 | 0.369 |
CLV_PCSK_SKI1_1 | 422 | 426 | PF00082 | 0.512 |
CLV_PCSK_SKI1_1 | 488 | 492 | PF00082 | 0.593 |
CLV_PCSK_SKI1_1 | 66 | 70 | PF00082 | 0.347 |
DEG_ODPH_VHL_1 | 354 | 367 | PF01847 | 0.466 |
DOC_CYCLIN_RxL_1 | 419 | 427 | PF00134 | 0.500 |
DOC_CYCLIN_RxL_1 | 509 | 520 | PF00134 | 0.466 |
DOC_MAPK_gen_1 | 38 | 46 | PF00069 | 0.417 |
DOC_PP1_RVXF_1 | 20 | 26 | PF00149 | 0.466 |
DOC_USP7_MATH_1 | 321 | 325 | PF00917 | 0.416 |
DOC_USP7_MATH_1 | 465 | 469 | PF00917 | 0.721 |
DOC_WW_Pin1_4 | 220 | 225 | PF00397 | 0.373 |
DOC_WW_Pin1_4 | 325 | 330 | PF00397 | 0.457 |
DOC_WW_Pin1_4 | 475 | 480 | PF00397 | 0.773 |
DOC_WW_Pin1_4 | 554 | 559 | PF00397 | 0.417 |
LIG_14-3-3_CanoR_1 | 300 | 309 | PF00244 | 0.466 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.305 |
LIG_BIR_III_2 | 476 | 480 | PF00653 | 0.761 |
LIG_BRCT_BRCA1_1 | 303 | 307 | PF00533 | 0.341 |
LIG_Clathr_ClatBox_1 | 156 | 160 | PF01394 | 0.417 |
LIG_deltaCOP1_diTrp_1 | 10 | 16 | PF00928 | 0.438 |
LIG_eIF4E_1 | 244 | 250 | PF01652 | 0.369 |
LIG_FHA_1 | 265 | 271 | PF00498 | 0.291 |
LIG_FHA_1 | 419 | 425 | PF00498 | 0.487 |
LIG_FHA_1 | 45 | 51 | PF00498 | 0.369 |
LIG_FHA_1 | 517 | 523 | PF00498 | 0.417 |
LIG_FHA_1 | 84 | 90 | PF00498 | 0.403 |
LIG_FHA_2 | 134 | 140 | PF00498 | 0.369 |
LIG_FHA_2 | 479 | 485 | PF00498 | 0.702 |
LIG_FHA_2 | 492 | 498 | PF00498 | 0.336 |
LIG_GBD_Chelix_1 | 510 | 518 | PF00786 | 0.466 |
LIG_LIR_Apic_2 | 427 | 431 | PF02991 | 0.556 |
LIG_LIR_Gen_1 | 223 | 234 | PF02991 | 0.466 |
LIG_LIR_Gen_1 | 439 | 449 | PF02991 | 0.581 |
LIG_LIR_Gen_1 | 47 | 56 | PF02991 | 0.429 |
LIG_LIR_Gen_1 | 505 | 516 | PF02991 | 0.420 |
LIG_LIR_Gen_1 | 541 | 552 | PF02991 | 0.417 |
LIG_LIR_Nem_3 | 223 | 229 | PF02991 | 0.417 |
LIG_LIR_Nem_3 | 273 | 277 | PF02991 | 0.369 |
LIG_LIR_Nem_3 | 335 | 340 | PF02991 | 0.395 |
LIG_LIR_Nem_3 | 439 | 444 | PF02991 | 0.517 |
LIG_LIR_Nem_3 | 47 | 51 | PF02991 | 0.466 |
LIG_LIR_Nem_3 | 505 | 511 | PF02991 | 0.420 |
LIG_LIR_Nem_3 | 541 | 547 | PF02991 | 0.417 |
LIG_MAD2 | 72 | 80 | PF02301 | 0.426 |
LIG_PCNA_yPIPBox_3 | 398 | 411 | PF02747 | 0.341 |
LIG_Pex14_1 | 11 | 15 | PF04695 | 0.535 |
LIG_Pex14_2 | 111 | 115 | PF04695 | 0.417 |
LIG_Pex14_2 | 303 | 307 | PF04695 | 0.291 |
LIG_SH2_CRK | 412 | 416 | PF00017 | 0.509 |
LIG_SH2_CRK | 428 | 432 | PF00017 | 0.526 |
LIG_SH2_CRK | 48 | 52 | PF00017 | 0.466 |
LIG_SH2_GRB2like | 15 | 18 | PF00017 | 0.486 |
LIG_SH2_NCK_1 | 48 | 52 | PF00017 | 0.466 |
LIG_SH2_NCK_1 | 493 | 497 | PF00017 | 0.466 |
LIG_SH2_STAP1 | 441 | 445 | PF00017 | 0.567 |
LIG_SH2_STAT5 | 15 | 18 | PF00017 | 0.536 |
LIG_SH2_STAT5 | 226 | 229 | PF00017 | 0.482 |
LIG_SH2_STAT5 | 244 | 247 | PF00017 | 0.171 |
LIG_SH2_STAT5 | 350 | 353 | PF00017 | 0.350 |
LIG_SH2_STAT5 | 360 | 363 | PF00017 | 0.310 |
LIG_SH2_STAT5 | 386 | 389 | PF00017 | 0.466 |
LIG_SH2_STAT5 | 423 | 426 | PF00017 | 0.464 |
LIG_SH2_STAT5 | 493 | 496 | PF00017 | 0.466 |
LIG_SH2_STAT5 | 556 | 559 | PF00017 | 0.417 |
LIG_SH3_3 | 169 | 175 | PF00018 | 0.363 |
LIG_SH3_3 | 447 | 453 | PF00018 | 0.599 |
LIG_SH3_3 | 455 | 461 | PF00018 | 0.623 |
LIG_SH3_3 | 520 | 526 | PF00018 | 0.417 |
LIG_SH3_3 | 544 | 550 | PF00018 | 0.466 |
LIG_SH3_3 | 74 | 80 | PF00018 | 0.439 |
LIG_TYR_ITIM | 410 | 415 | PF00017 | 0.511 |
LIG_TYR_ITIM | 46 | 51 | PF00017 | 0.466 |
LIG_UBA3_1 | 306 | 312 | PF00899 | 0.291 |
LIG_UBA3_1 | 50 | 59 | PF00899 | 0.369 |
MOD_CK1_1 | 325 | 331 | PF00069 | 0.465 |
MOD_CK1_1 | 472 | 478 | PF00069 | 0.753 |
MOD_CK1_1 | 5 | 11 | PF00069 | 0.398 |
MOD_CK1_1 | 538 | 544 | PF00069 | 0.341 |
MOD_CK2_1 | 230 | 236 | PF00069 | 0.466 |
MOD_CK2_1 | 252 | 258 | PF00069 | 0.350 |
MOD_CK2_1 | 49 | 55 | PF00069 | 0.482 |
MOD_CK2_1 | 491 | 497 | PF00069 | 0.388 |
MOD_GlcNHglycan | 166 | 169 | PF01048 | 0.432 |
MOD_GlcNHglycan | 212 | 215 | PF01048 | 0.390 |
MOD_GlcNHglycan | 231 | 235 | PF01048 | 0.437 |
MOD_GlcNHglycan | 254 | 257 | PF01048 | 0.369 |
MOD_GlcNHglycan | 291 | 294 | PF01048 | 0.466 |
MOD_GlcNHglycan | 4 | 7 | PF01048 | 0.436 |
MOD_GlcNHglycan | 470 | 474 | PF01048 | 0.599 |
MOD_GlcNHglycan | 51 | 54 | PF01048 | 0.370 |
MOD_GSK3_1 | 128 | 135 | PF00069 | 0.420 |
MOD_GSK3_1 | 260 | 267 | PF00069 | 0.433 |
MOD_GSK3_1 | 27 | 34 | PF00069 | 0.358 |
MOD_GSK3_1 | 321 | 328 | PF00069 | 0.460 |
MOD_GSK3_1 | 465 | 472 | PF00069 | 0.674 |
MOD_LATS_1 | 29 | 35 | PF00433 | 0.417 |
MOD_N-GLC_1 | 516 | 521 | PF02516 | 0.466 |
MOD_NEK2_1 | 133 | 138 | PF00069 | 0.377 |
MOD_NEK2_1 | 270 | 275 | PF00069 | 0.362 |
MOD_NEK2_1 | 302 | 307 | PF00069 | 0.341 |
MOD_NEK2_1 | 332 | 337 | PF00069 | 0.461 |
MOD_NEK2_1 | 424 | 429 | PF00069 | 0.490 |
MOD_NEK2_1 | 44 | 49 | PF00069 | 0.342 |
MOD_PKA_1 | 491 | 497 | PF00069 | 0.369 |
MOD_PKA_2 | 2 | 8 | PF00069 | 0.445 |
MOD_PKA_2 | 491 | 497 | PF00069 | 0.466 |
MOD_PKB_1 | 64 | 72 | PF00069 | 0.416 |
MOD_Plk_1 | 117 | 123 | PF00069 | 0.381 |
MOD_Plk_2-3 | 341 | 347 | PF00069 | 0.466 |
MOD_Plk_4 | 118 | 124 | PF00069 | 0.347 |
MOD_Plk_4 | 302 | 308 | PF00069 | 0.341 |
MOD_Plk_4 | 332 | 338 | PF00069 | 0.355 |
MOD_Plk_4 | 402 | 408 | PF00069 | 0.335 |
MOD_Plk_4 | 424 | 430 | PF00069 | 0.501 |
MOD_Plk_4 | 436 | 442 | PF00069 | 0.541 |
MOD_Plk_4 | 528 | 534 | PF00069 | 0.417 |
MOD_ProDKin_1 | 220 | 226 | PF00069 | 0.373 |
MOD_ProDKin_1 | 325 | 331 | PF00069 | 0.457 |
MOD_ProDKin_1 | 475 | 481 | PF00069 | 0.773 |
MOD_ProDKin_1 | 554 | 560 | PF00069 | 0.417 |
MOD_SUMO_for_1 | 265 | 268 | PF00179 | 0.291 |
MOD_SUMO_rev_2 | 369 | 378 | PF00179 | 0.466 |
MOD_SUMO_rev_2 | 463 | 471 | PF00179 | 0.598 |
MOD_SUMO_rev_2 | 484 | 490 | PF00179 | 0.570 |
TRG_ENDOCYTIC_2 | 226 | 229 | PF00928 | 0.466 |
TRG_ENDOCYTIC_2 | 412 | 415 | PF00928 | 0.518 |
TRG_ENDOCYTIC_2 | 441 | 444 | PF00928 | 0.517 |
TRG_ENDOCYTIC_2 | 48 | 51 | PF00928 | 0.417 |
TRG_ER_diArg_1 | 64 | 67 | PF00400 | 0.416 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I5C0 | Leptomonas seymouri | 36% | 94% |
A0A0S4IHN0 | Bodo saltans | 40% | 100% |
A0A0S4KND3 | Bodo saltans | 51% | 100% |
A0A1X0NPF8 | Trypanosomatidae | 56% | 84% |
A0A3S7WPX2 | Leishmania donovani | 100% | 85% |
A0A3S7X915 | Leishmania donovani | 34% | 100% |
A0A422MX37 | Trypanosoma rangeli | 33% | 86% |
A4HME0 | Leishmania braziliensis | 35% | 100% |
A4HME1 | Leishmania braziliensis | 35% | 100% |
A4IB13 | Leishmania infantum | 34% | 100% |
E9AEU2 | Leishmania major | 35% | 100% |
E9AL95 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
E9B5Z8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 100% |
F8DIF2 | Streptococcus parasanguinis (strain ATCC 15912 / DSM 6778 / CIP 104372 / LMG 14537) | 32% | 71% |
O13755 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 36% | 100% |
P0C278 | Shewanella frigidimarina | 33% | 99% |
P21375 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 33% | 100% |
P32614 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 33% | 100% |
P83223 | Shewanella oneidensis (strain MR-1) | 35% | 95% |
Q07WU7 | Shewanella frigidimarina (strain NCIMB 400) | 33% | 95% |
Q4QIK9 | Leishmania major | 95% | 100% |
Q8CVD0 | Shewanella oneidensis (strain MR-1) | 31% | 97% |
Q8DW88 | Streptococcus mutans serotype c (strain ATCC 700610 / UA159) | 28% | 71% |
Q9Z4P0 | Shewanella frigidimarina (strain NCIMB 400) | 31% | 96% |