GapMind for catabolism of small carbon sources

 

Alignments for a candidate for ARO8 in Saccharomonospora cyanea NA-134

Align Aromatic-amino-acid transaminase (EC 2.6.1.57) (characterized)
to candidate WP_005452808.1 SACCYDRAFT_RS01140 histidinol-phosphate transaminase

Query= reanno::BFirm:BPHYT_RS14905
         (370 letters)



>NCBI__GCF_000244975.1:WP_005452808.1
          Length = 351

 Score =  224 bits (571), Expect = 3e-63
 Identities = 141/333 (42%), Positives = 186/333 (55%), Gaps = 8/333 (2%)

Query: 37  VKLASNENPLGMPESAQRAMAQAASELGRYPDANAFELKAALSERYGVPADWVTLGNGSN 96
           VKLASNE P G   S   A+A+A+ E+ RYPD  A+ L   LS    VP   V +G GS 
Sbjct: 26  VKLASNEVPGGPLPSVADAIARASREINRYPDMGAWALVDRLSRELDVPTSQVAVGCGSV 85

Query: 97  DILEIAAHAFVEKGQSIVYAQYSFAVYALATQGLGARAIVVPAV-KYGHDLDAMLAAVSD 155
            + +    A    G  +++A  SF  Y + TQ   A  + VP    + HDLDAMLAA++ 
Sbjct: 86  SLCQQFVQALCAPGDEVLFAWRSFEAYPIVTQVGNATPVRVPLTPSHTHDLDAMLAAITP 145

Query: 156 DTRLIFVANPNNPTGTFIEGPKLEAFLDKVPRHVVVVLDEAYTEYLPQEKRYDSIAWVRR 215
            TRL+FV NPNNPTGT +   +L  FLD VP  VVVVLDEAY E++      D + + R 
Sbjct: 146 KTRLVFVCNPNNPTGTAVRRAELTRFLDNVPSDVVVVLDEAYREFVTDADVPDGLEFART 205

Query: 216 YPNLLVSRTFSKAFGLAGLRVGFAIAQPELTDLLNRVRQPFNVNTLAQAAAIAALNDKAF 275
            PN+ V RTFSKA+GLAGLRVG+A+A  E+ + + +V   F+VN LAQ AA+A+L+ K  
Sbjct: 206 RPNVAVLRTFSKAYGLAGLRVGYAVAADEVIEAVRKVYVAFSVNALAQTAALASLDAKDE 265

Query: 276 LEKSAALNAQGYRRLTEAFDKLGLEYVPSDGNFVLVRVGNDDAAGNRVNLELLKQGVIVR 335
           L    A       R+ E    LG E   +  NFV + +G    A    +LE     V+VR
Sbjct: 266 LLARCADIVAERTRVHETLRDLGYEVPETLANFVWLPLGERTTAFAEHSLE---HKVVVR 322

Query: 336 PVGNYGLPQWLRITIGLPEENEAFIAALERTLA 368
           P    G    +R+TIG  EEN+ F+ A    LA
Sbjct: 323 PFAGEG----VRVTIGTREENDTFLEAARAFLA 351


Lambda     K      H
   0.318    0.135    0.385 

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: 347
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: 370
Length of database: 351
Length adjustment: 29
Effective length of query: 341
Effective length of database: 322
Effective search space:   109802
Effective search space used:   109802
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