GapMind for catabolism of small carbon sources

 

Alignments for a candidate for pimB in Sphingopyxis indica DS15

Align 3-oxopimeloyl-CoA:CoA acetyltransferase (characterized)
to candidate WP_089216969.1 CHB69_RS16130 acetyl-CoA C-acyltransferase

Query= metacyc::MONOMER-20679
         (395 letters)



>NCBI__GCF_900188185.1:WP_089216969.1
          Length = 393

 Score =  475 bits (1223), Expect = e-139
 Identities = 247/393 (62%), Positives = 292/393 (74%), Gaps = 1/393 (0%)

Query: 1   MTEAVIVSTARTPIGKAYRGALNATEGATLLGHAIEHAVKRAGIDPKEVEDVVMGAAMQQ 60
           M +AVIVSTARTP+ KA RG+ N T   TL   +++ AV+RAG++  E++DVV GAAMQQ
Sbjct: 1   MRDAVIVSTARTPLTKAARGSFNNTPSPTLGAFSVKAAVERAGLEGGEIDDVVFGAAMQQ 60

Query: 61  GATGGNIARKALLRAGLPVTTAGTTIDRQCASGLQAIALAARSVLFDGVEIAVGGGGESI 120
           G+   N+AR   LRAGLPVT  G +IDRQC+SGL  IA AA+ ++ D  +I V GG ESI
Sbjct: 61  GSQSPNVARLIALRAGLPVTVPGMSIDRQCSSGLMTIATAAKQIIVDRQDICVAGGVESI 120

Query: 121 SLVQNDKMNTFHAVDPALEAIKGDVYMAMLDTAETVAKRYGISRERQDEYSLESQRRTAA 180
           S V       F   D  L A+  D YM M+ TAE VAKRY I RE QDEYSL+SQ+RTAA
Sbjct: 121 SKVSGSG-KVFIEPDAELLAMHKDTYMPMIGTAEVVAKRYNIGREAQDEYSLQSQQRTAA 179

Query: 181 AQQGGKFNDEIAPISTKMGVVDKATGAVSFKDITLSQDEGPRPETTAEGLAGLKAVRGEG 240
           AQ  GKF DEI P    M +VDK T  VS+KD+T  +DE  RP+TT EGLA LK V GEG
Sbjct: 180 AQAAGKFADEIIPCKATMAIVDKETKEVSYKDVTADRDECNRPDTTLEGLASLKPVMGEG 239

Query: 241 FTITAGNASQLSDGASATVIMSDKTAAAKGLKPLGIFRGMVSYGCEPDEMGIGPVFAVPR 300
            TITAGNASQLSDG+SA V+M  K A  +GL+PLG + GM   G EPDEMGIGPVFA+P+
Sbjct: 240 HTITAGNASQLSDGSSACVVMEAKVAEKRGLQPLGRYVGMAVAGTEPDEMGIGPVFAIPK 299

Query: 301 LLKRHGLSVDDIGLWELNEAFAVQVLYCRDKLGIDPEKLNVNGGAISVGHPYGMSGARLA 360
           LL+R  L +DDIGLWELNEAFAVQVLYCRDKLGI  E LNVNGG+IS+GHP+GM+GAR  
Sbjct: 300 LLERFELKMDDIGLWELNEAFAVQVLYCRDKLGIPNELLNVNGGSISIGHPFGMTGARCV 359

Query: 361 GHALIEGRRRKAKYAVVTMCVGGGMGSAGLFEI 393
           GHALIEG+RR  KYAVVTMC+GGG G+AGLFE+
Sbjct: 360 GHALIEGKRRGVKYAVVTMCIGGGQGAAGLFEV 392


Lambda     K      H
   0.316    0.134    0.378 

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: 476
Number of extensions: 15
Number of successful extensions: 2
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: 395
Length of database: 393
Length adjustment: 31
Effective length of query: 364
Effective length of database: 362
Effective search space:   131768
Effective search space used:   131768
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: 50 (23.9 bits)

This GapMind analysis is from Sep 24 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