Alignments for a candidate for leuA in Desulfobacter vibrioformis DSM 8776

GapMind for Amino acid biosynthesis

Alignments for a candidate for leuA in Desulfobacter vibrioformis DSM 8776

Align 2-isopropylmalate synthase; EC 2.3.3.13; Alpha-IPM synthase; Alpha-isopropylmalate synthase (uncharacterized)
to candidate WP_035240377.1 Q366_RS14820 homocitrate synthase

Query= curated2:B0TCR1
         (512 letters)



>NCBI__GCF_000745975.1:WP_035240377.1
          Length = 557

 Score =  221 bits (564), Expect = 4e-62
 Identities = 180/541 (33%), Positives = 262/541 (48%), Gaps = 53/541 (9%)

Query: 3   KRVVIFDTTLRDGEQSPGVSLNLHEKLEIAQQLARLGVDVIEAGFPIASPGDFEAVKAVA 62
           + V IFDTTLRDGEQ  GV+     KL IA+ LA  GV  IE GFP ++P +F+ VK +A
Sbjct: 24  QEVEIFDTTLRDGEQG-GVTFKGDSKLRIARFLADTGVSTIEVGFPSSTPLEFDTVKQIA 82

Query: 63  EQVRGPVICALARANRKDIERAAEALRGAEEARIHTFIATSPIHMQHKLRMEPDKVLDTA 122
           + V GP IC L   + ++I+R  +AL       IH F            + +P++ ++ A
Sbjct: 83  DTVEGPHICGLTTMDFENIKRTWQALENNPNPTIHVFTLNIDEASIRAYKADPNEQIEKA 142

Query: 123 VDAVKLAKSFTSN---VEFSAED-------AFRSDVGFL----CRIFSAAIEAGATTINI 168
             AV  AK  T     VEFSA++       +   +  FL      I+  AI+AGA  INI
Sbjct: 143 SRAVAYAKELTGGKGRVEFSAQNTILALSQSLNPEYSFLQEYISNIYGCAIKAGADVINI 202

Query: 169 PDTVGYATP---QEFGAFIKAIINGTPNIDKAIVSVHCHNDLGLAVANTLAALENGALQV 225
           P TV        QE   + K ++ GT   D  I+S H HND G++VA+TLAA+E G  QV
Sbjct: 203 PHTVAKGIEIEIQEAIQYFKMLVEGT---DDVILSFHAHNDFGVSVADTLAAVEQGIRQV 259

Query: 226 EGTINGIGERAGNASLEEVIMALYTRKPFYNLE--TSINKSEIYRTSRLVSNLTGMLVQP 283
           EGT   +GERAGN  LE+VIM L + KP YN +  T+         +R +   + + +  
Sbjct: 260 EGTWYSLGERAGNTPLEQVIMNL-SLKPSYNRKFFTAFKLERTNAVARFIERESSIPIPY 318

Query: 284 NKAIVGKNAFAHESGIHQDGVLKERTTYEIM----NPEMIGIFTNNIVLGKHSGRHAFRE 339
           N   +G NA  H SG+H DG  K +   E +    +PE IG   N   + K +G      
Sbjct: 319 NAPGIGPNALRHGSGVHSDGDKKGKAIGENIYLPCSPEDIGWTGNTHQITKLTGVAGVTA 378

Query: 340 RLKELGYSLDDEKLTKAFARFKALADRK-REIT--DEDLVVLVEDELRAFPEAYSLEYLH 396
           RL+ELG+  +     KAF R   + + K R+IT  D++L ++ +D      +    E   
Sbjct: 379 RLEELGFEFE-----KAFVREHIMPEIKSRDITYGDKELRMIGDDFRYTGKDHVEFEDYA 433

Query: 397 IT----SGTVLVPTATVRLRREEENFEEASCGDGPVDAAYKAIEKITGTG---ARLASYA 449
                 SG        + +  +++  E  +  +GP++A + AI+ +   G    +L  Y 
Sbjct: 434 FNKFAKSGDRHAQVVLI-IDGKKKTSEPFTGKNGPINAVFSAIDHVLELGDKKPKLVVYE 492

Query: 450 ISATTAGEDSQGEVSVKLEREGR---------FYTGRGVDTDIIVASAKAYLNAVNKIVF 500
            S       S  E  V L   G           + GR    D I ASAKAY+ A+++ + 
Sbjct: 493 PSNRGRTHSSAAEALVVLSGNGHELNYHLTAPVWVGRATHDDTITASAKAYVQALSRFMT 552

Query: 501 D 501
           D
Sbjct: 553 D 553


Lambda     K      H
   0.317    0.133    0.367 

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: 625
Number of extensions: 23
Number of successful extensions: 6
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 1
Length of query: 512
Length of database: 557
Length adjustment: 35
Effective length of query: 477
Effective length of database: 522
Effective search space:   248994
Effective search space used:   248994
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 Apr 10 2024. The underlying query database was built on Apr 09 2024.

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Steps (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 paper from 2022 on GapMind for carbon sources
the source code
instructions for running GapMind on your computer
changes to Amino acid biosynthesis since the publication.

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 Amino acid biosynthesis