GapMind for catabolism of small carbon sources

 

Alignments for a candidate for astE in Halomonas desiderata SP1

Align succinylglutamate desuccinylase (EC 3.5.1.96) (characterized)
to candidate WP_086508349.1 BZY95_RS02065 succinylglutamate desuccinylase

Query= BRENDA::O50177
         (332 letters)



>NCBI__GCF_002151265.1:WP_086508349.1
          Length = 328

 Score =  208 bits (529), Expect = 2e-58
 Identities = 137/329 (41%), Positives = 184/329 (55%), Gaps = 10/329 (3%)

Query: 4   LGKLLDLTLAGREPTEKI-QLTADGTRLHWLAEGALEVTPIGARDNGVDLLLSAGIHGNE 62
           L + ++L+L    P     +L     RLH  A G LE+TP   R      + S GIHGNE
Sbjct: 2   LSEWIELSLEETRPIASSGRLRGGSYRLH--APGILELTPTECRATARACVFSVGIHGNE 59

Query: 63  TAPIELLERLIRKVAAGTLKPAARVLFLFGNPEAIRRGERYVEQDMNRLFNGRHEEGSGN 122
           TAPIELL   + ++ AG L   A  L + GN EAIRR ERYV  ++NRLF  R  + +G 
Sbjct: 60  TAPIELLGNCLARIEAGLLPLGAPALIILGNLEAIRRAERYVNTNLNRLFR-RDLDETGM 118

Query: 123 EAFRAAELERLAQVFFSK-TERVHLHYDLHTAIRGSKIEQFALYPWAEGRQHSRSELAR- 180
           E  RA +L      F+++ + R  LHYDLHTAIR S+  +F + P+A      R E  R 
Sbjct: 119 EPDRARQLMSAVDDFYARHSGRERLHYDLHTAIRDSRFPRFVVEPFA--ATPIRPEQWRW 176

Query: 181 LRDAGIEAVLLQNKPGITFSAYTYGQLGAEAFTLELGKARPFGENQEVNLERLERSLELL 240
           L +AGI+AVL Q++   TFS Y+     A+AFTLELG+A PFG N    L  + R LE L
Sbjct: 177 LAEAGIQAVLHQHRHSWTFSHYSKHYHQAQAFTLELGRALPFGHNDLTALAPMTRLLEAL 236

Query: 241 IDGSEEQPDGSRLDGLKLFSVSREVIKHSDHFRLHLDDDVANFTELSPGYLLAEDIGGTR 300
           ++G E  P G+    +  F V+ E+++ S  FRL   DD  NFTE +PG  LAED     
Sbjct: 237 LEGRE--PRGADPARMAFFRVAHELMRQSQDFRLCFPDDTPNFTEFAPGTRLAEDASAGP 294

Query: 301 WVVDEVGARIIFPNPRVKNGLRAGILVVP 329
           + V +    ++FPN  V+ G RA +L  P
Sbjct: 295 FTVQDEPLSVVFPNAAVELGARAALLARP 323


Lambda     K      H
   0.319    0.138    0.399 

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: 327
Number of extensions: 11
Number of successful extensions: 4
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: 332
Length of database: 328
Length adjustment: 28
Effective length of query: 304
Effective length of database: 300
Effective search space:    91200
Effective search space used:    91200
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 (21.7 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Sep 24 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