GapMind for catabolism of small carbon sources

 

Alignments for a candidate for astE in Pseudomonas stutzeri RCH2

Align Succinylglutamate desuccinylase (EC 3.5.1.96) (characterized)
to candidate GFF2664 Psest_2717 Succinylglutamate desuccinylase

Query= reanno::pseudo13_GW456_L13:PfGW456L13_1977
         (336 letters)



>FitnessBrowser__psRCH2:GFF2664
          Length = 332

 Score =  322 bits (826), Expect = 6e-93
 Identities = 178/329 (54%), Positives = 223/329 (67%), Gaps = 5/329 (1%)

Query: 1   MLALGKLLELTLAGREPAEKTQLTVEGVRMRWLSEGALEVRPPEARDNGLDLLLSAGIHG 60
           MLALGKLLELTLAGREP EK QLT  GV++ WL++GAL V PP  +D GLDLLLSAGIHG
Sbjct: 1   MLALGKLLELTLAGREPCEKVQLTPRGVKLHWLADGALLVSPPPGQDQGLDLLLSAGIHG 60

Query: 61  NETAPIELLDRLLHDIARGDLKPRARILFLFGNPEAIRKGERFVEQDVNRLFNGRHEQSS 120
           NE  PI +LDRL+  +AR D++PRA +L LF NP A+R+  R VE D+NRLF G H    
Sbjct: 61  NELIPIHVLDRLVRALARDDVRPRAPLLLLFANPAAMRRMVRQVEHDLNRLFRGEHADVW 120

Query: 121 GCEALRACELERLAASFFSLPDRQRLHYDLHTAIRGSKIEQFALYPWKEDRQHSRQELAR 180
           G EA+RA ELE L   FFS   RQR HYDLH+A+R S++ QFA+ PW+E  Q S + L R
Sbjct: 121 GGEAIRAAELEALVGGFFSGAGRQRRHYDLHSALRPSRLAQFAICPWRECEQVSAESLTR 180

Query: 181 LRAAGMEAVLLQNKPSIVFSSYTYDKLGAEAFTLELGKARPFGQNDGVNVSLLEKRLKQI 240
           L    +E VLLQ + +  FS+ T  + GAEAFTLEL  A   G++  V V   E+ L  +
Sbjct: 181 LDRLAIEGVLLQRQATSTFSAMTSTRYGAEAFTLEL--AEGAGESLPVAVVQFERGLYGM 238

Query: 241 IEGTEPELTEDALDGLQLYSVAREIIKHSDSFRLNLPADIENFSELEVGYLLAEDIANTR 300
           IEG E  +   AL   QL  ++RE+IK S  FRL +P+DIENF+ L +G +LAED    R
Sbjct: 239 IEGREAPVAAHALP--QLLQISREVIKRSPRFRLCVPSDIENFAPLPLGSVLAED-DGAR 295

Query: 301 WIIEEEGARIIFPNPRVKNGLRAGILVVP 329
           W+I+E GARI+FP   V  G RA ++VVP
Sbjct: 296 WVIDEPGARILFPMADVAEGQRAALIVVP 324


Lambda     K      H
   0.319    0.138    0.394 

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: 299
Number of extensions: 16
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: 336
Length of database: 332
Length adjustment: 28
Effective length of query: 308
Effective length of database: 304
Effective search space:    93632
Effective search space used:    93632
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 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