GapMind for Amino acid biosynthesis

 

Alignments for a candidate for leuC in Shewanella loihica PV-4

Align 3-isopropylmalate dehydratase large subunit 2; EC 4.2.1.33; Alpha-IPM isomerase 2; IPMI 2; Isopropylmalate isomerase 2 (uncharacterized)
to candidate 5209348 Shew_1822 aconitate hydratase (RefSeq)

Query= curated2:Q9WZ24
         (417 letters)



>FitnessBrowser__PV4:5209348
          Length = 862

 Score =  117 bits (293), Expect = 1e-30
 Identities = 111/344 (32%), Positives = 156/344 (45%), Gaps = 48/344 (13%)

Query: 114 DLVVGADSHTCTYGALGAFATGVGSTDIAGFYLIGKVWFRVPESIKVTLRGKFKDLVTAK 173
           D +VG DSHT    ALG  A GVG  +     L    + R+P+ + V L GK +  +TA 
Sbjct: 194 DTLVGTDSHTPHVDALGVIAIGVGGLEAENVMLGRPSYMRLPDIVGVELTGKRQSGITAT 253

Query: 174 DLVLKLISILGVDGANYKAIEFSGPGVKEISMDGRFTISNMAIEAGGKTGLFPVDEITIA 233
           D+VL L   L  +      +EF G G  ++++  R TISNM  E G   G+F +D+ TI 
Sbjct: 254 DIVLALTEFLRQEKVVSAYLEFFGEGAADLTLGDRATISNMTPEFGASAGMFYIDQQTID 313

Query: 234 YERERGIEVEE------------MYPD--EDAKYVREVEMDLSELEPQVAYPFLPSNAKD 279
           Y    G + E+            ++ D  +DA+Y R +  DLS +   +A P  P     
Sbjct: 314 YLTITGRDSEQVKLVENYAKTTGLWADSLKDAEYERVLTFDLSSVVRNIAGPSNPHRRVA 373

Query: 280 VSEAEKERIK--IDQ------------AVIGSCTNGRIEDLRLAAQILK------GRTVS 319
            SE   + I   ++Q            A I SCTN       +AA +L       G    
Sbjct: 374 TSELASQGIAGVVEQDDKLMPDGAVIIAAITSCTNTSNPRNVIAAGLLAKKANELGLVRK 433

Query: 320 PDVRCIIIPGSQKVYKQALKE-GLIDIFIDAGCAVSTPTCGPCLG--GHMGVLAEGEV-- 374
           P V+    PGS KV +  LK+ GL+      G  +    C  C G  G +  + + EV  
Sbjct: 434 PWVKTSFAPGS-KVAELYLKDAGLLPELEQLGFGIVGFACTTCNGMSGALDPVIQQEVID 492

Query: 375 ------AISTTNRNFVGRMGHPNSK-VFLASPAVAAASAIKGYI 411
                 A+ + NRNF GR+ HP +K  FLASP +  A AI G I
Sbjct: 493 RDLYATAVLSGNRNFDGRI-HPYAKQAFLASPPLVVAYAIAGTI 535


Lambda     K      H
   0.318    0.138    0.395 

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: 716
Number of extensions: 39
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: 417
Length of database: 862
Length adjustment: 37
Effective length of query: 380
Effective length of database: 825
Effective search space:   313500
Effective search space used:   313500
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 (21.7 bits)
S2: 53 (25.0 bits)

This GapMind analysis is from Apr 09 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