Aligments for a candidate for lutB in Pseudomonas fluorescens FW300-N2C3

GapMind for catabolism of small carbon sources

Aligments for a candidate for lutB in Pseudomonas fluorescens FW300-N2C3

Align Iron-sulfur cluster binding protein (characterized, see rationale)
to candidate AO356_07560 AO356_07560 (Fe-S)-binding protein

Query= uniprot:E4PLR6
         (483 letters)



>FitnessBrowser__pseudo5_N2C3_1:AO356_07560
          Length = 489

 Score =  744 bits (1922), Expect = 0.0
 Identities = 369/478 (77%), Positives = 407/478 (85%), Gaps = 2/478 (0%)

Query: 5   IPVTELTPDFRGRAEEALADGQLRNNFRVAMDSLMTKRANAFPDADEREGLRELGNRIKA 64
           +PV E   DFR RA +AL D QLRNNFR AMDSLMTKRA +F DA ERE LR LGN ++A
Sbjct: 12  VPV-EAQEDFRARAHKALDDTQLRNNFRSAMDSLMTKRAASFSDAHEREHLRVLGNAVRA 70

Query: 65  GALSRLPDLLEQLEQKLTENGVKVHWAETVEEANSLVHGIIEARKGSQVVKGKSMVSEEM 124
            ALS+LPDLLEQLE  LT NGV VHWAETV+EAN +V  II A +  QV+KGKSMVSEEM
Sbjct: 71  RALSKLPDLLEQLETNLTRNGVNVHWAETVDEANGIVLSIIRAHEARQVIKGKSMVSEEM 130

Query: 125 EMNDYLAERGVECLESDMGEYIVQLDNEKPSHIIMPAIHKNARQVSKLFHDKLGEPETED 184
           EMN +L  R +ECLESDMGEYIVQLD+EKPSHIIMPAIHKNA QV+ LFHDKLG   T+D
Sbjct: 131 EMNHFLEARDIECLESDMGEYIVQLDHEKPSHIIMPAIHKNAGQVASLFHDKLGVEYTKD 190

Query: 185 VNQLIQIGRRTLRRKFMEADVGVSGVNFAIAETGTLLLVENEGNGRMSTTAPPVHIAVTG 244
           V+QLIQIGR+ LR+KF EAD+GVSGVNFA+AETGTLLLVENEGNGRMSTT PPVHIAVTG
Sbjct: 191 VDQLIQIGRKVLRQKFFEADIGVSGVNFAVAETGTLLLVENEGNGRMSTTVPPVHIAVTG 250

Query: 245 IEKVVPNLRDVVPLVSLLTRSALGQPITTYVNLISGPRKPDELDGPEEVHLVLLDNGRTG 304
           IEKVV NLRDVVPL+SLLTRSALGQPITTYVN+ISGPRK DELDGP+EVHLVLLDNGR+ 
Sbjct: 251 IEKVVENLRDVVPLLSLLTRSALGQPITTYVNMISGPRKADELDGPQEVHLVLLDNGRSQ 310

Query: 305 AFADAQMRQTLNCIRCGACMNHCPVYTRVGGHTYGEVYPGPIGKIITPHMAGLDKVPDHP 364
           AFAD+++RQTLNCIRCGACMNHCPVYTR+GGH YGEVYPGPIGKIITPHM GL KVPDHP
Sbjct: 311 AFADSELRQTLNCIRCGACMNHCPVYTRIGGHAYGEVYPGPIGKIITPHMVGLAKVPDHP 370

Query: 365 SASSLCGACGEVCPVKIPIPELLQRLRQENVKNPEQPQQV-KGGGAKYSRTERWIWRGWQ 423
           SASSLCGACGEVCPVKIPIP LL+RLR+ENVK P+ P QV +G G+KYS  ER+IW  W 
Sbjct: 371 SASSLCGACGEVCPVKIPIPALLRRLREENVKAPDSPNQVMRGQGSKYSPKERFIWNAWA 430

Query: 424 MLNTRPALYRSFLWAATRFRALAPKKAGPWTENHSAPVPARRSLHDLAARHLDQNGGR 481
            LN+ P LYR F + ATR RAL PK  GPWT+NHSAP PA RSLHDLA  HL+Q GGR
Sbjct: 431 WLNSSPRLYRLFGFLATRLRALTPKNLGPWTQNHSAPQPAARSLHDLAREHLNQQGGR 488


Lambda     K      H
   0.317    0.135    0.403 

Gapped
Lambda     K      H
   0.267   0.0410    0.140 


Matrix: BLOSUM62
Gap Penalties: Existence: 11, Extension: 1
Number of Sequences: 1
Number of Hits to DB: 753
Number of extensions: 28
Number of successful extensions: 4
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 1
Number of HSP's successfully gapped: 1
Length of query: 483
Length of database: 489
Length adjustment: 34
Effective length of query: 449
Effective length of database: 455
Effective search space:   204295
Effective search space used:   204295
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.6 bits)
S2: 52 (24.6 bits)

This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.

Downloads

Candidates (tab-delimited)
Steps (tab-delimited)
Rules (tab-delimited)
Protein sequences (fasta format)
Organisms (tab-delimited)
SQLite3 databases

Related tools

About GapMind

Each pathway is defined by a set of rules based on individual steps or genes. Candidates for each step are identified by using ublast (a fast alternative to protein BLAST) against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer with enzyme models (usually from TIGRFam). Ublast hits may be split across two different proteins.

A candidate for a step is "high confidence" if either:

ublast finds a hit to a characterized protein at above 40% identity and 80% coverage, and bits >= other bits+10.
- (Hits to curated proteins without experimental data as to their function are never considered high confidence.)
HMMer finds a hit with 80% coverage of the model, and either other identity < 40 or other coverage < 0.75.

where "other" refers to the best ublast hit to a sequence that is not annotated as performing this step (and is not "ignored").

Otherwise, a candidate is "medium confidence" if either:

ublast finds a hit at above 40% identity and 70% coverage (ignoring otherBits).
ublast finds a hit at above 30% identity and 80% coverage, and bits >= other bits.
HMMer finds a hit (regardless of coverage or other bits).

Other blast hits with at least 50% coverage are "low confidence."

Steps with no high- or medium-confidence candidates may be considered "gaps." For the typical bacterium that can make all 20 amino acids, there are 1-2 gaps in amino acid biosynthesis pathways. For diverse bacteria and archaea that can utilize a carbon source, there is a complete high-confidence catabolic pathway (including a transporter) just 38% of the time, and there is a complete medium-confidence pathway 63% of the time. Gaps may be due to:

our ignorance of proteins' functions,
omissions in the gene models,
frame-shift errors in the genome sequence, or
the organism lacks the pathway.

GapMind relies on the predicted proteins in the genome and does not search the six-frame translation. In most cases, you can search the six-frame translation by clicking on links to Curated BLAST for each step definition (in the per-step page).

For more information, see the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.

If you notice any errors or omissions in the step descriptions, or any questionable results, please let us know

by Morgan Price, Arkin group, Lawrence Berkeley National Laboratory

GapMind for catabolism of small carbon sources