GapMind for catabolism of small carbon sources

 

Alignments for a candidate for prpC in Pseudomonas stutzeri RCH2

Align 2-methylcitrate synthase (EC 2.3.3.5) (characterized)
to candidate GFF2275 Psest_2320 2-methylcitrate synthase/citrate synthase II

Query= BRENDA::Q9I5E3
         (375 letters)



>FitnessBrowser__psRCH2:GFF2275
          Length = 375

 Score =  628 bits (1620), Expect = 0.0
 Identities = 308/375 (82%), Positives = 338/375 (90%)

Query: 1   MAEAKVLSGAGLRGQVAGQTALSTVGQEGAGLTYRGYDVRDLAAAAIFEEVAYLLLYGEL 60
           MAEAKVLSGAGLRGQ+AGQTAL TVG+ GAGLTYRGYDVRDLAA   FEEVAYLL YGEL
Sbjct: 1   MAEAKVLSGAGLRGQIAGQTALCTVGKTGAGLTYRGYDVRDLAAECDFEEVAYLLFYGEL 60

Query: 61  PNKQQLDAYLKKLQGQRDLPQALKEVLERIPKDAHPMDVMRTGASVLGTLEPELSFDQQR 120
           P  QQL  Y  +L+  RDLPQALKEVLERIP +AHPMDVMRTG+SVLGTLEPE+SF+QQR
Sbjct: 61  PTAQQLADYKNRLKTMRDLPQALKEVLERIPANAHPMDVMRTGSSVLGTLEPEVSFEQQR 120

Query: 121 DVADRLLAAFPAIMTYWYRFTHEGQRIDCNSDEPTIGGHFLALLHGKKPSELHVKVMNVS 180
           DVA+RL+AAFPAIM YWYRFTH+G RI+C SDE T+GGHFLALLH KKPS+LHVKVMNVS
Sbjct: 121 DVAERLMAAFPAIMCYWYRFTHDGVRINCTSDEDTLGGHFLALLHDKKPSDLHVKVMNVS 180

Query: 181 LILYAEHEFNASTFTARVCASTLSDLYSCVTGAIGSLRGPLHGGANEAAMELIERFSSPQ 240
           LILYAEHEFNASTFTARVCASTLSDLYSCVTGAIGSLRGPLHGGANEAAM++IE+++SP+
Sbjct: 181 LILYAEHEFNASTFTARVCASTLSDLYSCVTGAIGSLRGPLHGGANEAAMDMIEQWTSPE 240

Query: 241 EATAELLKMLERKDKIMGFGHAIYKDSDPRNEVIKGWSKQLADEVGDKVLFAVSEAIDKT 300
           EA   +L MLERKDKIMGFGHAIY  SDPRNEVIK W+K+LADEVGD VL+ VS A+D+T
Sbjct: 241 EAREAILGMLERKDKIMGFGHAIYSVSDPRNEVIKVWAKKLADEVGDTVLYPVSVAVDET 300

Query: 301 MWEQKKLFPNADFYHASAYHFMGIPTKLFTPIFVCSRTSGWTAHVFEQRANNRIIRPSAE 360
           MWEQKKLFPNADFYHASAYHFMGIPTKLFTPIFVCSR +GW +HVFEQR+NNRIIRPSAE
Sbjct: 301 MWEQKKLFPNADFYHASAYHFMGIPTKLFTPIFVCSRVTGWASHVFEQRSNNRIIRPSAE 360

Query: 361 YTGVEQRAFVPLEQR 375
           Y G EQR  VP+ QR
Sbjct: 361 YIGPEQRKVVPIAQR 375


Lambda     K      H
   0.319    0.134    0.396 

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: 554
Number of extensions: 13
Number of successful extensions: 1
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: 375
Length of database: 375
Length adjustment: 30
Effective length of query: 345
Effective length of database: 345
Effective search space:   119025
Effective search space used:   119025
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.

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