GapMind for Amino acid biosynthesis

 

Alignments for a candidate for tyrB in Leptospirillum ferrooxidans C2-3

Align branched-chain-amino-acid aminotransferase; EC 2.6.1.42 (characterized)
to candidate WP_014448409.1 LFE_RS00950 branched-chain amino acid transaminase

Query= CharProtDB::CH_024500
         (309 letters)



>NCBI__GCF_000284315.1:WP_014448409.1
          Length = 311

 Score =  274 bits (700), Expect = 2e-78
 Identities = 145/304 (47%), Positives = 198/304 (65%), Gaps = 10/304 (3%)

Query: 4   KKADYIWFNGEMVRWEDAKVHVMSHALHYGTSVFEGIRCYDSHKGPVVFRHREHMQRLHD 63
           K++ +IW +G+MV W+DA VHV++H+LHYG +VFEGIR Y   +G  +FR  EH +RL +
Sbjct: 3   KESQWIWMDGKMVPWKDANVHVLTHSLHYGMAVFEGIRAYSGPEGTSIFRLAEHTRRLVN 62

Query: 64  SAKIYRFPVSQSIDELMEACRDVIRKNNLTSAYIRPLIFVGDVGMGV----NPPAGYSTD 119
           S K+       S +ELM+A   V+R+NNL+S YIRPL++VG   MG+    NP       
Sbjct: 63  SGKVMLMKSPYSEEELMDATCRVVRENNLSSCYIRPLMYVGYGDMGIYARQNPIC----- 117

Query: 120 VIIAAFPWGAYLGAEALEQGIDAMVSSWNRAAPNTIPTAAKAGGNYLSSLLVGSEARRHG 179
           V I+A+ WG YLG E L +GI A +SS++R   NT    AK   +Y++S L   E +  G
Sbjct: 118 VSISAWEWGTYLGEEGLSKGIRAKISSFSRFGVNTFLNRAKVSAHYVNSQLAKWEVKMAG 177

Query: 180 YQEGIALDVNGYISEGAGENLFEVKDGVLFTPPFTSSALPGITRDAIIKLAKELGIEVRE 239
           Y E I LD +G+++EG GEN+F V  GVL TP    + L GITR+A+  LAKE+GI V E
Sbjct: 178 YDEAILLDQDGFVAEGPGENIFIVSGGVLRTPAL-KTVLDGITRNAVQTLAKEMGIPVWE 236

Query: 240 QVLSRESLYLADEVFMSGTAAEITPVRSVDGIQVGEGRCGPVTKRIQQAFFGLFTGETED 299
            VL+R+ LYLADE F +GTAAE+TP+R +D   +G GR GPVT  +Q+AFF +  G  +D
Sbjct: 237 GVLTRDDLYLADEAFFTGTAAELTPIREIDERTIGTGRPGPVTLALQKAFFDVVHGHVKD 296

Query: 300 KWGW 303
              W
Sbjct: 297 HSEW 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: 315
Number of extensions: 7
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: 309
Length of database: 311
Length adjustment: 27
Effective length of query: 282
Effective length of database: 284
Effective search space:    80088
Effective search space used:    80088
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 Jul 25 2024. The underlying query database was built on Jul 25 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