GapMind for catabolism of small carbon sources

 

Alignments for a candidate for ans in Sphingomonas histidinilytica UM2

Align beta-aspartyl-peptidase (EC 3.4.19.5); asparaginase (EC 3.5.1.1) (characterized)
to candidate WP_079650106.1 B5X82_RS20870 isoaspartyl peptidase/L-asparaginase

Query= BRENDA::P37595
         (321 letters)



>NCBI__GCF_900167915.1:WP_079650106.1
          Length = 318

 Score =  247 bits (630), Expect = 3e-70
 Identities = 140/306 (45%), Positives = 185/306 (60%), Gaps = 10/306 (3%)

Query: 6   IAIHGGAGAISRAQMSLQQELRYIEALSAIVETGQKMLEAGESALDVVTEAVRLLEECPL 65
           + IHGGAG + R  +    E      L+A ++ G  +L  G +A+D V  AVR+LE+ P 
Sbjct: 20  LVIHGGAGQLRRLLLGSDAEAHATTVLTAALDAGATILAGGGTAVDAVEAAVRVLEDDPY 79

Query: 66  FNAGIGAVFTRDETHELDACVMDGNTLKAGAVAGVSHLRNPVLAARLVMEQSPHVMMIGE 125
           FNAG GAVF+ D  +ELDA +MDG T +AGAV+ V+  RNPV  AR VMEQSPHVM+   
Sbjct: 80  FNAGRGAVFSADGINELDAAIMDGATREAGAVSAVTKARNPVTLARAVMEQSPHVMLTAS 139

Query: 126 GAENFAFARGMERVSPEIFSTSLRYEQLLAARKEGATVLDHSGAPLDEKQKMGTVGAVAL 185
           GA+ F     +E+V+P  F T  R+ Q    R         +G   D   K GTVGAVA 
Sbjct: 140 GADRFGAEHDIEQVAPAWFHTDERWRQYEELR---------AGGTFDADLKYGTVGAVAR 190

Query: 186 DLDGNLAAATSTGGMTNKLPGRVGDSPLVGAGCYANNASVAVSCTGTGEVFIRALAAYDI 245
           D  G LAAATSTGG+T K   R+GDSP++GAG +A +A  A SCTG+GE FIR  AA+++
Sbjct: 191 DDKGRLAAATSTGGLTGKRWNRIGDSPVIGAGTWAEDAGAATSCTGSGEHFIRVGAAHEL 250

Query: 246 AALMDYGGLSLAEACERVVMEKLPALGGSGGLIAIDHEGNVALPFNTEGMYRAWGYAGDT 305
           +A +   G S+ EA   V+ E + ALGG GGLI++D +G     FN++GMYR    A   
Sbjct: 251 SARVRLAGQSIGEAGAGVIGE-IGALGGIGGLISVDAQGRGGWCFNSQGMYRGLARADQP 309

Query: 306 PTTGIY 311
               +Y
Sbjct: 310 HIVAMY 315


Lambda     K      H
   0.316    0.133    0.377 

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: 349
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: 321
Length of database: 318
Length adjustment: 28
Effective length of query: 293
Effective length of database: 290
Effective search space:    84970
Effective search space used:    84970
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: 48 (23.1 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