GapMind for Amino acid biosynthesis

 

Alignments for a candidate for leuC in Methylomicrobium alcaliphilum 20Z

Align 3-isopropylmalate dehydratase large subunit; EC 4.2.1.33; Alpha-IPM isomerase; IPMI; Isopropylmalate isomerase (uncharacterized)
to candidate WP_014146819.1 MEALZ_RS01520 aconitate hydratase AcnA

Query= curated2:Q2G958
         (478 letters)



>NCBI__GCF_000968535.2:WP_014146819.1
          Length = 899

 Score =  125 bits (314), Expect = 6e-33
 Identities = 107/359 (29%), Positives = 166/359 (46%), Gaps = 29/359 (8%)

Query: 138 DSHTACHGGLGALAFGIGTSEVEHVLATQTLLLKQSKTMEVRVEGELTPGVTAKDVVLHI 197
           DSHT    GLG LA+G+G  E E V+  Q + + +   + +++ G+L PGVTA D+VL I
Sbjct: 211 DSHTPMVNGLGVLAWGVGGIEAEAVILDQPIYMLEPDVVGIKLTGKLPPGVTATDLVLRI 270

Query: 198 TGVLGAAGGTGSVIEYTGSVIRDLSIEGRLTISNMAIEHGARAGLCAPDEKTFAYLKGRP 257
           T +    G  G  +E+ GS +  LSI  R TISNMA E G+       D+    Y++   
Sbjct: 271 TELCRQFGVVGQFVEFYGSGLSQLSIPDRATISNMAPEQGSTVSFFPVDKAALNYMRLTG 330

Query: 258 YAPRGEDWDKAVAWWKSL-ATD--PGATYDKVVVIDAKDIAPSVTWGTSPEDVLPISGLV 314
            +P   +  +  A  + L  TD  P   + + + +D  +I P++     P+D +P+S + 
Sbjct: 331 RSPEQIELTERYAKLQGLFRTDDAPEPEFTRTLEVDLGEIEPALAGPKRPQDRIPLSQVG 390

Query: 315 PA-PESFADP---SKQEAARASLEYMGLVPG----QRMEDVEVQNIFIGSCTNSRIEDMR 366
           P   ++   P        A + L+  G+V      + +    V    I SCTN+    + 
Sbjct: 391 PTYRQTLIAPVGIRGMGLAESDLDRCGVVSNKGACETITHGAVVIAAITSCTNTSNPSVM 450

Query: 367 AAA------AILKGRKKADNVKWAIVVPGSGLVKKQAEEEGLDRVFIEAGFEWREPGCSA 420
             A      A+ KG K  + VK ++  PGS +V +  ++ GL       GF     GC+ 
Sbjct: 451 LGAGLVAKKAVEKGLKVKNYVKTSL-APGSQVVTEYLKQSGLLPYLEALGFYLVGYGCTT 509

Query: 421 CLG-MNPDKVPAGERCAS---------TSNRNFVGRQGPGART-HLVSPAMAAAAAVTG 468
           C+G   P  V   E             + NRNF GR  P  +T +L SP +  A A+ G
Sbjct: 510 CIGNSGPLDVAVEEAIVDNDLVVSAVLSGNRNFEGRVHPLTKTNYLASPPLVVAYALAG 568


Lambda     K      H
   0.317    0.134    0.399 

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: 1041
Number of extensions: 62
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: 478
Length of database: 899
Length adjustment: 38
Effective length of query: 440
Effective length of database: 861
Effective search space:   378840
Effective search space used:   378840
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: 54 (25.4 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