GapMind for Amino acid biosynthesis

 

Alignments for a candidate for hcs in Dechlorosoma suillum PS

Align Homocitrate synthase; EC 2.3.3.14 (uncharacterized)
to candidate Dsui_3227 Dsui_3227 2-isopropylmalate synthase

Query= curated2:P05345
         (381 letters)



>FitnessBrowser__PS:Dsui_3227
          Length = 560

 Score = 70.1 bits (170), Expect = 1e-16
 Identities = 93/348 (26%), Positives = 136/348 (39%), Gaps = 40/348 (11%)

Query: 9   TTLRDGEQSPGVAFRTSEKVAIAEALYAAGITAMEVGTPAMG--DEEIARIQLVRRQLP- 65
           T LRDG QS        +K+ + + L   G   +EV  P+    D    R  +    +P 
Sbjct: 36  TDLRDGNQSLFEPMNVEKKMRMFKTLCQVGFKEIEVAFPSASQTDFNFVRSLIEDGHIPQ 95

Query: 66  DATL--MTWCRMNALEIRQSADLGIDWVDISI------PASDKLRQYKLREPLAVLLERL 117
           D T+  +T  R + +     +  G     + +      P  D +      E +A+ +E +
Sbjct: 96  DVTIEVLTQAREHLIRRTMESIKGAPRAIVHVYNATSQPFRDFVFGMSKAEVVAMAVEAV 155

Query: 118 AMFIHLAHTLGLKVCIGCEDASRASGQTLRAIAEVAQNAPAAR---------LRYADTVG 168
            +   LA  +     +        +   L    EV     AA          L    TV 
Sbjct: 156 TLIKQLAAEMPETEVVLEYSPETFTATELDFALEVCDAVTAAWGATPDNKVILNLPTTVE 215

Query: 169 LLDPFTTAAQIS------ALRDVWSGEIEMHAHNDLGMATANTLAAVSAGATSVNTTVLG 222
           +  P   A QI       A RD  S  + +H HND G A A     + AGA  V   + G
Sbjct: 216 MATPNIYADQIEWMHRHLARRD--SVILSLHPHNDRGTAVAAAELGLMAGADRVEGCLFG 273

Query: 223 LGERAGNAAAWKPSALGLERCLGVETGVHFSALPALCQRVAEAAQRAIDPQQPLVGELVF 282
            GER GN       AL +    GV  G+ FS + A+ + V    Q  I P+ P VG+LVF
Sbjct: 274 NGERTGNVDI-VTVALNMYT-QGVHPGLDFSDINAVARTVEHCNQLPIHPRHPYVGDLVF 331

Query: 283 THESGVHVAALLRDSES----------YQSIAPSLMGRSYRLVLGKHS 320
           T  SG H  A+ +   +          Y  I P+ +GRSY  V+  +S
Sbjct: 332 TAFSGSHQDAIKKGFSAQKADAPWNVPYLPIDPADVGRSYDSVIRVNS 379


Lambda     K      H
   0.319    0.132    0.384 

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: 378
Number of extensions: 20
Number of successful extensions: 3
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: 381
Length of database: 560
Length adjustment: 33
Effective length of query: 348
Effective length of database: 527
Effective search space:   183396
Effective search space used:   183396
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: 51 (24.3 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