GapMind for catabolism of small carbon sources

 

Alignments for a candidate for kbl in Pedobacter sp. GW460-11-11-14-LB5

Align 2-amino-3-ketobutyrate coenzyme A ligase (EC 2.3.1.29) (characterized)
to candidate CA265_RS02025 CA265_RS02025 8-amino-7-oxononanoate synthase

Query= reanno::ANA3:7026975
         (397 letters)



>FitnessBrowser__Pedo557:CA265_RS02025
          Length = 413

 Score =  203 bits (517), Expect = 6e-57
 Identities = 119/366 (32%), Positives = 195/366 (53%), Gaps = 11/366 (3%)

Query: 37  IQVNHQEVVNFCANNYLGLANHPELIKAAQQGLDSHGFGMA---SVRFICGTQDIHKQLE 93
           +Q   +E + +  NNYLGLANHPE+ KA ++      FGMA     R + G  + H+QLE
Sbjct: 38  MQFRGKEHLVWSLNNYLGLANHPEVRKADEEAAAK--FGMAYPMGARMMSGNSNYHEQLE 95

Query: 94  ASLSEFLGMEDTILYSSCFDANAGLFETLLDAEDAIISDALNHASIIDGVRLCKAKRFRY 153
             L+EF+G  D  L +  +     + +TL+D  D ++ DA +HA I+DG+RL   KRF Y
Sbjct: 96  QELAEFVGKPDAFLLNYGYQGMVSIIDTLVDRNDVVVYDAESHACIVDGLRLHMGKRFVY 155

Query: 154 ANNDMADLETQLIAAK---AAGARNILIATDGVFSMDGVIANLQGVCDLADKYGALVMVD 210
            +ND+     QL  A          IL+ T+GVF M G    L+ + DL   +   ++VD
Sbjct: 156 KHNDIESARKQLERATKLVEETGGGILLITEGVFGMSGAQGKLKEIVDLKKDFNFRILVD 215

Query: 211 DSHAVGFVGLNGRGSHEHCGVMGRVDIITGTLGKALGGASGGFTSGKKEVIDWLRQRSRP 270
           D+H  G +G  G G+HE    +  +D+  GT  K++ G  G F +  +++ ++LR   R 
Sbjct: 216 DAHGFGTMGKTGAGTHEAQDCIEGIDVYFGTFAKSMAGI-GAFVASTEQITNFLRYNMRS 274

Query: 271 YLFSNSLAPSIVTASIHVLEMLKSGQALREAVWENSRYFREKMSAAGFTLGGADHAIIPV 330
             F+ +L   +V   +  LE+LKS   L++ +WE +   ++ +   GF LG  D  + PV
Sbjct: 275 QTFAKALPMPMVIGLLKRLELLKSKPELKDKLWEIAMTLQKGLRERGFDLGVTDSVVTPV 334

Query: 331 MI-GDAKLASDFANRLLAEH-IYVIGFSFPVVPKGQARIRTQMSAAHTREQLDKAIEAFT 388
            + G+   A+     L   + I+     +PV+PKG   +R   +A HT E + + ++AF+
Sbjct: 335 FLKGELSDATAITYDLRENYSIFCSIVVYPVIPKGMIELRLIPTAVHTLEDVQRTLDAFS 394

Query: 389 RIAKEM 394
            +A+++
Sbjct: 395 EVAEKL 400


Lambda     K      H
   0.321    0.134    0.385 

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: 402
Number of extensions: 23
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: 397
Length of database: 413
Length adjustment: 31
Effective length of query: 366
Effective length of database: 382
Effective search space:   139812
Effective search space used:   139812
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 (21.9 bits)
S2: 50 (23.9 bits)

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

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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