GapMind for catabolism of small carbon sources

 

Alignments for a candidate for D-LDH in Pseudomonas fluorescens GW456-L13

Align D-lactate dehydrogenase (EC 1.1.1.28) (characterized)
to candidate PfGW456L13_1617 D-3-phosphoglycerate dehydrogenase (EC 1.1.1.95)

Query= BRENDA::F8A9V0
         (325 letters)



>FitnessBrowser__pseudo13_GW456_L13:PfGW456L13_1617
          Length = 321

 Score =  137 bits (345), Expect = 4e-37
 Identities = 100/303 (33%), Positives = 149/303 (49%), Gaps = 22/303 (7%)

Query: 16  LGPILPSDWDVEMTPDFLDETTVEKAKGAQVVSLFVSDKADGPVLEALHSYGVGLLALRS 75
           L P+     D+++    L +  +E  KGA V    +S+K          S  + L+ + +
Sbjct: 22  LDPLRSCFGDLQLFAQTLPDQVIEHLKGATVA---ISNKILIDAAAMAASPDLKLILITA 78

Query: 76  AGYDHIDIETAKRLGIKVVNVPAYSPHAIADHTLAIMLALIRRLHRAHDKVRLG------ 129
            G +++D+  A+  GI V N   Y   ++A HT+ ++L L  RL      V  G      
Sbjct: 79  TGTNNVDLAAARAHGITVCNCQGYGTPSVAQHTIMLLLNLATRLADYQKAVGEGRWQQAK 138

Query: 130 DFDLDGLMGFDLNGKVAGVIGLGKIGRLVATRLKAFGCKV-LGYDPYIQPEIVENVDLDT 188
            F L      +L GK  G++G G++G  VA   +AFG +V LG  P  +P   + + LD 
Sbjct: 139 QFCLLDYPIVELEGKTLGLLGHGELGGAVARLAEAFGMRVVLGQIPG-RPARPDRLPLDE 197

Query: 189 LITQADIISIHCPLTRENFHMFNEETFKRMKPGAILVNTARGGLIDTKALLEALKSGKLG 248
           L+ Q D +++HCPL     H         MKPGA +VNTARGGLID +AL  AL++G LG
Sbjct: 198 LLPQVDALTLHCPLNEHTRHFIGARELAAMKPGAFVVNTARGGLIDEQALANALRNGHLG 257

Query: 249 GAALDVYEYERGLFFKNHQKEGIKDPYLAQLLGLANVVLTGHQAFLTREAVKNIEETTVE 308
           GAA DV   E  +           +P LA    +  +++T H A+ +REA + I     E
Sbjct: 258 GAATDVLSVEPPV---------NGNPLLAH--DIPRLIVTPHNAWGSREARQRIVGQVTE 306

Query: 309 NIL 311
           N L
Sbjct: 307 NAL 309


Lambda     K      H
   0.321    0.140    0.407 

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: 210
Number of extensions: 10
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: 325
Length of database: 321
Length adjustment: 28
Effective length of query: 297
Effective length of database: 293
Effective search space:    87021
Effective search space used:    87021
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: 48 (23.1 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