GapMind for catabolism of small carbon sources

 

Alignments for a candidate for aruG in Halomonas desiderata SP1

Align arginine N-succinyltransferase (EC 2.3.1.109) (characterized)
to candidate WP_086508152.1 BZY95_RS01055 arginine N-succinyltransferase

Query= BRENDA::P80358
         (340 letters)



>NCBI__GCF_002151265.1:WP_086508152.1
          Length = 348

 Score =  286 bits (731), Expect = 7e-82
 Identities = 157/343 (45%), Positives = 217/343 (63%), Gaps = 12/343 (3%)

Query: 1   MIVRPVTSADLPALIELARSTGTGLTTLPANEQRLQHRVSWAEKAFRGEAERGDADYLFV 60
           M +RP+   DL  L ++AR TG G T+LP N + L  +++ A  AF         +Y FV
Sbjct: 1   MRIRPIAEGDLDELQKIARETGVGFTSLPDNREFLAAKIAAAVAAFEQRTPADRRNYFFV 60

Query: 61  LEDD-AGKVVGISAIAGAVGLREPWYNYRVGLTVSASQELNIHREIPTLFLANDLTGNSE 119
           LED+ +G++ G  AI G VG   P+Y+YR+G    +S +L++HR I TLFL++D TG++E
Sbjct: 61  LEDEESGELAGCCAIEGQVGREVPFYHYRLGTLAHSSVQLDLHRTIDTLFLSSDHTGDAE 120

Query: 120 LCSLFLHADHRSG-----LNGKLLSRARFLFIAEFRHLFGDKLIAEMRGMSDEEGRSPFW 174
           + SLFL    R        NG LLS  R+LF+AEFR  F DK++AEMRG+ DE G+SPFW
Sbjct: 121 VASLFLRPGFRGKERAHQRNGALLSMVRWLFMAEFRDQFPDKVLAEMRGVFDERGKSPFW 180

Query: 175 ESLGRHFFKMEFSQADYLTGVGNKAFIAELMPKFPLYTCFLSEEARGVIGRVHPNTEPAL 234
           E LG HFF ++F +AD LTG+G K+FI ELMPKFP+YT FLS+EAR  IG+VH +T PAL
Sbjct: 181 ECLGSHFFPLDFDEADRLTGLGQKSFIGELMPKFPIYTPFLSDEARACIGQVHHDTRPAL 240

Query: 235 AMLKAEGFSYQGYVDIFDAGPAIEAETDKIRAIAESQNLVLAVGTPGDDAEP----YLIH 290
           AMLK EG  ++GY+DIFD GP +EA  D +RA+ +S    + + + G D  P    +L  
Sbjct: 241 AMLKKEGLRWEGYIDIFDGGPTVEAYIDDVRAVRKSHCCRVEIRS-GSDTPPARPRWLAA 299

Query: 291 NRKREDCRIT-AAPARAAAGTLVVDPLTAKRLRLSAGASVRAV 332
           +    + R    A      GTL +    A+RL ++AG S+R +
Sbjct: 300 STTMAEFRAAWVACGPDEEGTLTLSETEAQRLGVAAGDSLRVL 342


Lambda     K      H
   0.320    0.136    0.398 

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: 336
Number of extensions: 18
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: 340
Length of database: 348
Length adjustment: 29
Effective length of query: 311
Effective length of database: 319
Effective search space:    99209
Effective search space used:    99209
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: 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