GapMind for catabolism of small carbon sources

 

Alignments for a candidate for lysN in Burkholderia phytofirmans PsJN

Align L-2-aminoadipate aminotransferase monomer (EC 2.6.1.39) (characterized)
to candidate BPHYT_RS05965 BPHYT_RS05965 2-aminoadipate aminotransferase

Query= metacyc::MONOMER-6727
         (397 letters)



>FitnessBrowser__BFirm:BPHYT_RS05965
          Length = 398

 Score =  337 bits (864), Expect = 4e-97
 Identities = 182/397 (45%), Positives = 255/397 (64%), Gaps = 13/397 (3%)

Query: 1   MKPLSWSEAFGKSAGRIQASTIRELLKLTQRPGILSFAGGLPAPELFPKEEAAEAAARIL 60
           +K  +W     + A ++ +S IRE+LK+T+RP ++SFAGGLP+P  FP E    A+ RIL
Sbjct: 6   LKAPTWQ--LSERARKLTSSAIREILKVTERPEVISFAGGLPSPATFPAERMRAASDRIL 63

Query: 61  REKGEVALQYSPTEGYAPLRAFVAEWIGV-----RPEEVLITTGSQQALDLVGKVFLDEG 115
           R++   ALQYS TEG+ PLR ++A+   V     RP +VLITTGSQQALDL+GKV +   
Sbjct: 64  RDEPAAALQYSATEGFLPLREWIAKRYSVNGAQIRPTQVLITTGSQQALDLLGKVLVCPD 123

Query: 116 SPVLLEAPSYMGAIQAFRLQGPRFLTVPAGEEGPDLDALEEVLKRERPRFLYLIPSFQNP 175
           SPVL+E P+Y+GA+Q+F +  PR++ VP  E G   + L   L     R LY  P+FQNP
Sbjct: 124 SPVLVETPTYLGALQSFSMYEPRYVQVPTDEHGLVPEGLTPELTAGA-RLLYAQPNFQNP 182

Query: 176 TGGLTPLPARKRLLQMVMERGLVVVEDDAYRELYFGEARLPSLFELAREAGYPGVIYLGS 235
           TG   P+  R+ L          V+EDD Y  L +    LP++  +A +     +++LGS
Sbjct: 183 TGRRLPIERRRALAAFAKTAPFPVIEDDPYGALDYAGEPLPTMLSMAPDH----IVHLGS 238

Query: 236 FSKVLSPGLRVAFAVAHPEALQKLVQAKQGADLHTPMLNQMLVHELLKEGFSE-RLERVR 294
           FSKVL+PGLRV + +A  E + KLVQAKQ  DLHTP   Q +V+E++K+GF +  +  +R
Sbjct: 239 FSKVLAPGLRVGYIIAPEELIFKLVQAKQATDLHTPSFTQRIVYEVIKDGFLDTHVPTIR 298

Query: 295 RVYREKAQAMLHALDREVPKEVRYTRPKGGMFVWMELPKGLSAEGLFRRALEENVAFVPG 354
            +YR++  AML +L+R +P+ V + RP+GGMFVW+ LP  + +  L   A+ +NVAFVPG
Sbjct: 299 ELYRDQCAAMLASLERYMPEGVSWNRPEGGMFVWVNLPAQIDSMKLLEEAVAQNVAFVPG 358

Query: 355 GPFFANGGGENTLRLSYATLDREGIAEGVRRLGRALK 391
           GPFFAN    NTLRLS+ T+    I EGV RLG  ++
Sbjct: 359 GPFFANEAQHNTLRLSFVTVPPARIDEGVSRLGALIR 395


Lambda     K      H
   0.320    0.139    0.401 

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: 508
Number of extensions: 19
Number of successful extensions: 5
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: 397
Length of database: 398
Length adjustment: 31
Effective length of query: 366
Effective length of database: 367
Effective search space:   134322
Effective search space used:   134322
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: 50 (23.9 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