GapMind for Amino acid biosynthesis

 

Alignments for a candidate for argE'B in Klebsiella variicola At-22

Align N-succinylcitrulline desuccinylase (EC 3.5.1.-) (characterized)
to candidate WP_012968216.1 KVAR_RS12925 M20 family metallopeptidase

Query= reanno::Btheta:353076
         (355 letters)



>NCBI__GCF_000025465.1:WP_012968216.1
          Length = 380

 Score = 98.2 bits (243), Expect = 3e-25
 Identities = 97/366 (26%), Positives = 152/366 (41%), Gaps = 33/366 (9%)

Query: 13  VSLLKSLISIPSISR--EETQAADFLQNYIEAEGMQT-----GRKGNNVWCLSPMFDLKK 65
           + L + L+   +I+    E     F  ++++  G +      G    N+    P     K
Sbjct: 5   LELARQLLGFNTINPPGSEADCMRFFADWLDESGFEVSLSSFGEGRCNLIASLPGAKSGK 64

Query: 66  PTILLNSHIDTVKPVNG-WRKDPFTPREENGKLYGLGSNDAGASVVSLLQVFLQLCRTSQ 124
           P +    H+DTV   N  W+ DPF  + E+G+LYG GS+D  A++ +     +       
Sbjct: 65  P-LAFTGHLDTVPLGNARWQYDPFGSQMEDGRLYGRGSSDMKAAIAAFAVACVHQREAIL 123

Query: 125 NYNLIYLASCEEEVSGKEGIESVLPG--LPPVSFAIVGEPTEMQPAIAEKGLMVLDVTAT 182
                 L     E +G +G  +++    LP V   IVGEPT   P I  KG + L     
Sbjct: 124 AGRGAVLLITGGEETGCDGARALIASATLPEVGALIVGEPTANYPVIGHKGALWLRCETR 183

Query: 183 GKAGHAARDE-GDNAIYKVLNDIAWFRDYRFEKESPLLGPVKMSVTVINAGTQHNVVPDK 241
           GK  H A  E G NAIY   + +   + +      PL+    ++V  I  G   N VPD+
Sbjct: 184 GKTAHGAMPELGINAIYLAADALGKIQHFSPGAPHPLMKQPTLNVGRIEGGLNINSVPDR 243

Query: 242 CTFVVDIRSNELYSNEDLFAEIRKHIA------------CDAKARSFRLNSSRIDEKHPF 289
             F VDIRS     +    A IR+ +              D  A   R + + I + +  
Sbjct: 244 TRFDVDIRSAPNLQH----ATIRERLTTLLGESVTVSTLVDLPAVLSREDHAWIKQVYQR 299

Query: 290 VQKAVKMGRIPFGSPTLSDQALMSFA-----SVKIGPGRSSRSHTAEEYIMLKEIEEAIG 344
            Q        P   P  +D +L+  A      + +GPG  S +H  +EY +L  + EA  
Sbjct: 300 CQPLHAEPIAPRVVPYFTDASLLLPALGDPPCIILGPGEPSMAHQTDEYCLLSRLAEAEQ 359

Query: 345 IYLDLL 350
           +Y D++
Sbjct: 360 LYGDII 365


Lambda     K      H
   0.317    0.134    0.387 

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: 283
Number of extensions: 11
Number of successful extensions: 4
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 2
Length of query: 355
Length of database: 380
Length adjustment: 30
Effective length of query: 325
Effective length of database: 350
Effective search space:   113750
Effective search space used:   113750
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.6 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Jul 25 2024. The underlying query database was built on Jul 25 2024.

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