GapMind for Amino acid biosynthesis

 

Alignments for a candidate for leuB in Desulfatiglans anilini DSM 4660

Align 3-isopropylmalate dehydrogenase; 3-IPM-DH; Beta-IPM dehydrogenase; IMDH; EC 1.1.1.85 (characterized)
to candidate WP_028320142.1 H567_RS0102190 3-isopropylmalate dehydrogenase

Query= SwissProt::P9WKK9
         (336 letters)



>NCBI__GCF_000422285.1:WP_028320142.1
          Length = 354

 Score =  300 bits (767), Expect = 5e-86
 Identities = 172/345 (49%), Positives = 218/345 (63%), Gaps = 16/345 (4%)

Query: 3   LAIIAGDGIGPEVTAEAVKVLDAVVPGVQKT----SYDLGARRFHATGEVLPDSVVAELR 58
           + +I GDG GPEV AE +K L+A       T     YDLG   +   G +LPDSV+ ELR
Sbjct: 7   IGVIPGDGTGPEVVAEGLKALEAAGRKHDLTFDFKRYDLGGEAYLRDGTLLPDSVIHELR 66

Query: 59  NHDAILLGAIGDPSVPSGVLERGLLLRLRFELDHHINLRPARLYPGVASPLSGNP--GID 116
             DAI LGAIG P V  G+LER +LL+LRFELD +INLRP  L+PGV +PL G     ID
Sbjct: 67  GMDAIFLGAIGHPGVKPGILEREVLLKLRFELDLYINLRPVVLHPGVDTPLMGKQPEDID 126

Query: 117 FVVVREGTEGPYTGNGGAIRVGTPNEVATEVSVNTAFGVRRVVADAFERARRRRK--HLT 174
           FVVVRE +EG Y G GG  + GT +EVA + SVNT  GV R +  AFE AR+R K  H+T
Sbjct: 127 FVVVRENSEGMYAGGGGFFKKGTADEVAIQESVNTRKGVERCIRYAFEYARKRNKGKHVT 186

Query: 175 LVHKTNVLTFAGGLWLRTVDEVGECYPDVEVAYQHVDAATIHMITDPGRFDVIVTDNLFG 234
           L  KTNVL F   LW R   +V + +PD+   YQHVDA  + MI +P +FDVIVT NLFG
Sbjct: 187 LCAKTNVLIFESDLWFRVFQDVAKDFPDIGTGYQHVDALCMWMIKNPEQFDVIVTGNLFG 246

Query: 235 DIITDLAAAVCGGIGLAASGNIDATRANPSMFEPVHGSAPDIAGQGIADPTAAIMSVALL 294
           DIITD+ A + GG+G+AA GNI   ++  +MFEP+ GSAP   GQ   +P AAI S  +L
Sbjct: 247 DIITDIGAIIQGGLGIAAGGNIHPGQS--AMFEPIGGSAPKYTGQNKINPMAAIGSAQML 304

Query: 295 LSHLGEHDAAARVDRAVEAHLA------TRGSERLATSDVGERIA 333
           L +LG+  AAA + +A+   L+        G     TS+VG+ +A
Sbjct: 305 LEYLGKDKAAADIFQAIRKVLSQDLKSLEAGRMGYTTSEVGDLVA 349


Lambda     K      H
   0.319    0.137    0.398 

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: 356
Number of extensions: 18
Number of successful extensions: 5
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: 336
Length of database: 354
Length adjustment: 29
Effective length of query: 307
Effective length of database: 325
Effective search space:    99775
Effective search space used:    99775
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: 49 (23.5 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