GapMind for catabolism of small carbon sources

 

Alignments for a candidate for kbl in Bacteroides thetaiotaomicron VPI-5482

Align 2-amino-3-ketobutyrate coenzyme A ligase (EC 2.3.1.29) (characterized)
to candidate 350971 BT1443 8-amino-7-oxononanoate synthase (NCBI ptt file)

Query= reanno::Koxy:BWI76_RS27255
         (397 letters)



>FitnessBrowser__Btheta:350971
          Length = 384

 Score =  193 bits (491), Expect = 6e-54
 Identities = 119/353 (33%), Positives = 192/353 (54%), Gaps = 6/353 (1%)

Query: 35  DITVGGSQVINFCANNYLGLANHPELIAAAKSGMDSHGF--GMASVRFICGTQDSHKALE 92
           D+TV G +++N  +N+YLGLAN   L  A    +    F    +S R + G   +++ LE
Sbjct: 31  DVTVDGRRMLNLSSNDYLGLANEVSLREAFLKTITPETFLPTSSSSRLLTGNFTAYQELE 90

Query: 93  KKLADFLGMEDAILYSSCFDANGGLFETLLGAEDAIISDALNHASIIDGVRLCKAKRFRY 152
           ++LA   G E A+L++S + AN G+   +  A   I++D L HAS+IDG+RL  AK  RY
Sbjct: 91  QQLATMFGAESALLFNSGYHANTGILPAVSDARTLILADKLVHASLIDGIRLSSAKCIRY 150

Query: 153 ANNDMVELEARLKEARDAGARHVLIATDGVFSMDGVIANLKGVCDLADKY-DALVMVDDS 211
            +ND+ +L  RL E        ++I T+ +FSMDG  A+L+ +  L   Y + L+ VD++
Sbjct: 151 RHNDLAQLR-RLLEENHGMYEKIIIVTESIFSMDGDEADLQALVRLKHDYANLLLYVDEA 209

Query: 212 HAVGFVGENGRGSHEYCDVMGRVDIITGTLGKALGGASGGYTAARKEVVEWLRQRSRPYL 271
           HA G  GE G G  E  + +  +D + GT GKA   A G Y   R+ + E+L  + R ++
Sbjct: 210 HAFGARGEKGLGCAEEQNCINDIDFLVGTFGKAAASA-GAYIICRQTIREYLINKMRTFI 268

Query: 272 FSNSLAPAIVAASIKVLEMVEAGSELRDRLWSNARLFREKMTAAGFILAGADHAIIPVML 331
           F+ +L P  +  +  VL+        R+ L   +R  +E +T  G+      H I+P+++
Sbjct: 269 FTTALPPVNIQWTAWVLKHFADFRSKREHLLQISRKLKEALTEKGYNCPSVSH-IVPMVV 327

Query: 332 GEATVAQEFARELQKEGIYVTGFFYPVVPKGQARIRTQMSAAHTPEQIERAVE 384
           G +      A ELQ++G Y      P VP+G +RIR  ++A  T ++I+  +E
Sbjct: 328 GASEDTIRKAEELQRKGFYALPVRPPTVPEGTSRIRFSLTADITEKEIDTLIE 380


Lambda     K      H
   0.321    0.136    0.390 

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: 300
Number of extensions: 17
Number of successful extensions: 6
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: 397
Length of database: 384
Length adjustment: 31
Effective length of query: 366
Effective length of database: 353
Effective search space:   129198
Effective search space used:   129198
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: 50 (23.9 bits)

This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.

Links

Downloads

Related tools

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