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

GapMind for catabolism of small carbon sources

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

Align methylcrotonoyl-CoA carboxylase (subunit 2/2) (EC 6.4.1.4) (characterized)
to candidate AO356_02930 AO356_02930 3-methylcrotonyl-CoA carboxylase

Query= BRENDA::Q9I299
         (655 letters)



>lcl|FitnessBrowser__pseudo5_N2C3_1:AO356_02930 AO356_02930
           3-methylcrotonyl-CoA carboxylase
          Length = 656

 Score =  563 bits (1450), Expect = e-164
 Identities = 315/657 (47%), Positives = 418/657 (63%), Gaps = 18/657 (2%)

Query: 7   SIQRLLVANRGEIACRVMRSARALGIGSVAVHSDIDRHARHVAEADIAVDLGGAKPADSY 66
           +  ++L+ANRGEIACR+ R+A+ALG  +VAV S+ D  A HV  AD AV +G A    SY
Sbjct: 3   AFSKILIANRGEIACRIQRTAQALGYRTVAVFSEADADALHVRMADEAVLIGAAPVQQSY 62

Query: 67  LRGDRIIAAALASGAQAIHPGYGFLSENADFARACEEAGLLFLGPPAAAIDAMGSKSAAK 126
           L    I+ AA  SGA AIHPGYGFLSENA FA AC +AGL+F+GP   AI+ MGSK  AK
Sbjct: 63  LDPRVILEAARRSGADAIHPGYGFLSENARFAHACAQAGLVFIGPSPEAIELMGSKRRAK 122

Query: 127 ALMEEAGVPLVPGYHGEAQDLETFRREAGRIGYPVLLKAAAGGGGKGMKVVEREAELAEA 186
             M +AGVP + GY G AQD +T +REAGRIGYP+++KA+AGGGG+GM++V+R  +L E 
Sbjct: 123 IAMIQAGVPCIAGYQGAAQDDDTLQREAGRIGYPLMIKASAGGGGRGMRLVQRAEDLLEQ 182

Query: 187 LSSAQREAKAAFGDARMLVEKYLLKPRHVEIQVFADRHGHCLYLNERDCSIQRRHQKVVE 246
           L SA+ EA   FG   +++E+ L+ PRHVE+Q+F D HG  ++L ERDCSIQRRHQK++E
Sbjct: 183 LRSARSEALHGFGSDELILEQALIDPRHVEVQIFGDHHGQLIHLGERDCSIQRRHQKIIE 242

Query: 247 EAPAPGLGAELRRAMGEAAVRAAQAIGYVGAGTVEFLLDERGQFFFMEMNTRLQVEHPVT 306
           EAP P + A+LRRAMGEAA+ A  A+ YVGAGTVEFLL   G+F+F+EMNTRLQVEHPVT
Sbjct: 243 EAPCPVMTADLRRAMGEAALTAGHAVNYVGAGTVEFLLAADGRFYFLEMNTRLQVEHPVT 302

Query: 307 EAITGLDLVAWQIRVARGEALPLTQEQVPLNGHAIEVRLYAEDPEGDFLPASGRLMLYRE 366
           E+ITGLDLVAWQ+ VA G+ LPL QEQV L+GHA++VRLYAEDP  DFLP +G L+ + E
Sbjct: 303 ESITGLDLVAWQLDVATGKPLPLCQEQVTLSGHALQVRLYAEDPAADFLPQTGCLVGW-E 361

Query: 367 AAAGPGRRVDSGVREGDEVSPFYDPMLAKLIAWGETREEARQRLLAMLAETSVGGLRTNL 426
                G RVD G+ +G  ++PFYD ML KLI  G TR+EAR++LL  + +  + G+++N 
Sbjct: 362 PPIRDGVRVDHGLLQGQAITPFYDSMLGKLIVHGATRDEARRKLLRAVEDCVLLGVQSNQ 421

Query: 427 AFLRRILGHPAFAAAELDTGFIARH---QDDLLPAPQALPE------HFWQAAAEAWLQS 477
             L  +L HP F   + +TGFI++H      LLP   ++ +       F+QA+       
Sbjct: 422 RLLAGLLAHPRFIDGDFNTGFISQHFANHAALLPLEPSVEQLAIATAAFYQASQARHAPG 481

Query: 478 EPGHRRDDDPHSPWSRNDG---WRSALARESDLMLRCRDERRCVRLRHASPSQYRLDGDD 534
             G R        +    G   W  +L  E+D  L  R + R + LR        +D   
Sbjct: 482 LGGWRNSIGTALHYRIGVGERDWVLSLETETDGTLNIRSDGRLIELRLLD-----VDAQG 536

Query: 535 LVSRVDGVTRRSAALRRGRQLFLEWEGELLAIEAVDPIAEAEAAHAHQGGLSAPMNGSIV 594
               +DG+ +R A    G  L+L      L ++       A  A A    L APM+G+IV
Sbjct: 537 ATLVIDGIGQRHAWHLEGHDLWLSTRPGGLHLQDRTLAPVASKASAGASTLLAPMDGAIV 596

Query: 595 RVLVEPGQTVEAGATLVVLEAMKMEHSIRAPHAGVVKALYCSEGELVEEGTPLVELD 651
            VLV  G  V  G  L+VLEAMKMEH ++A   GVV+ L  + G+ V +   L+ ++
Sbjct: 597 EVLVSEGSPVRQGQLLMVLEAMKMEHPLKAGSDGVVRQLQATRGDQVRKRQVLLRIE 653


Lambda     K      H
   0.319    0.135    0.397 

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: 1070
Number of extensions: 41
Number of successful extensions: 3
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: 655
Length of database: 656
Length adjustment: 38
Effective length of query: 617
Effective length of database: 618
Effective search space:   381306
Effective search space used:   381306
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.8 bits)
S2: 54 (25.4 bits)

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

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Candidates (tab-delimited)
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Protein sequences (fasta format)
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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 preprint 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