GapMind for Amino acid biosynthesis

 

Alignments for a candidate for tyrB in Chlorobium phaeobacteroides BS1

Align branched-chain-amino-acid aminotransferase; EC 2.6.1.42 (characterized)
to candidate WP_012474057.1 CPHAMN1_RS03045 branched-chain amino acid transaminase

Query= CharProtDB::CH_024500
         (309 letters)



>NCBI__GCF_000020545.1:WP_012474057.1
          Length = 303

 Score =  332 bits (852), Expect = 5e-96
 Identities = 162/301 (53%), Positives = 215/301 (71%), Gaps = 4/301 (1%)

Query: 5   KADYIWFNGEMVRWEDAKVHVMSHALHYGTSVFEGIRCYDSHKGPVVFRHREHMQRLHDS 64
           K++ IW NGE+V W DAK+H++SH +HYG+S FEGIRCY++ KGP +    EH++RL+DS
Sbjct: 3   KSEKIWMNGELVDWNDAKIHILSHVIHYGSSTFEGIRCYETTKGPAILFLDEHIRRLYDS 62

Query: 65  AKIYRFPVSQSIDELMEACRDVIRKNNLTSAYIRPLIFVGDVGMGVNPPAGYSTDVIIAA 124
           +KIYR  +  S+ E+  A  D I+ N   S YIRPL++ G   +GVNP    + +V IA 
Sbjct: 63  SKIYRIEIPYSMAEIRTAVIDTIKANGHKSCYIRPLVYRGQGALGVNPHLA-AIEVAIAT 121

Query: 125 FPWGAYLGAEALEQGIDAMVSSWNRAAPNTIPTAAKAGGNYLSSLLVGSEARRHGYQEGI 184
           + WG YLG + LE G+D  VSSWNR APNT+PT AKAGGNYL+S L+  EA    Y EGI
Sbjct: 122 WEWGTYLGEDVLETGVDVRVSSWNRLAPNTLPTWAKAGGNYLNSQLIKMEAIMDNYAEGI 181

Query: 185 ALDVNGYISEGAGENLFEVKDGVLFTPPFTSSALPGITRDAIIKLAKELGIEVREQVLSR 244
            LD+NGY+SEG+GEN+F ++DG+++TP    S L G+TR AII +AKELG EVRE ++ R
Sbjct: 182 GLDINGYVSEGSGENIFIIRDGIIYTPMTGQSVLAGLTRQAIIHIAKELGYEVRETMIPR 241

Query: 245 ESLYLADEVFMSGTAAEITPVRSVDGIQVGEGRCGPVTKRIQQAFFGLF-TGETEDKWGW 303
           E+LY+ADEVF++GTAAEITPVRS+D   VG    GPVT+ +Q  +  +  TG  ED + W
Sbjct: 242 EALYIADEVFLTGTAAEITPVRSIDKHPVGNEIRGPVTEILQSHYLKIIQTG--EDPYNW 299

Query: 304 L 304
           L
Sbjct: 300 L 300


Lambda     K      H
   0.319    0.136    0.413 

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: 313
Number of extensions: 5
Number of successful extensions: 2
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: 309
Length of database: 303
Length adjustment: 27
Effective length of query: 282
Effective length of database: 276
Effective search space:    77832
Effective search space used:    77832
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: 48 (23.1 bits)

This GapMind analysis is from Apr 10 2024. The underlying query database was built on Apr 09 2024.

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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:

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:

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:

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:

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