GapMind for catabolism of small carbon sources

 

Alignments for a candidate for pimB in Methylobacterium nodulans ORS 2060

Align 3-oxopimeloyl-CoA:CoA acetyltransferase (characterized)
to candidate WP_015929439.1 MNOD_RS13390 3-oxoadipyl-CoA thiolase

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



>NCBI__GCF_000022085.1:WP_015929439.1
          Length = 404

 Score =  242 bits (618), Expect = 1e-68
 Identities = 168/405 (41%), Positives = 219/405 (54%), Gaps = 32/405 (7%)

Query: 3   EAVIVSTARTPIGKAYRGALNATEGATLLGHAIEHAVKRAGIDPKEVEDVVMGAAMQQGA 62
           +  I    RTPIG+ Y GAL +     L    +   + R       VE+V +G A Q G 
Sbjct: 6   DVYICDFVRTPIGR-YGGALASVRADDLAAIPLAALLHRNPSLKDGVEEVFLGCANQAGE 64

Query: 63  TGGNIARKALLRAGLPVTTAGTTIDRQCASGLQAIALAARSVLFDGVEIAVGGGGESISL 122
              N+AR ALL AGLP T  G T++R CASGL A+  AAR++    +++A+ GG ES++ 
Sbjct: 65  DNRNVARMALLLAGLPETVPGLTLNRLCASGLDAVGAAARAIRSGDIDLALAGGVESMTR 124

Query: 123 VQ----------------NDKMNTFHAVDPALEAIKGDVYMAMLDTAETVAKRYGISRER 166
                             +D    +  ++P L+   G    +M +TAE VA+ + ISR  
Sbjct: 125 APFVMGKSEGAWQRQAEIHDTTIGWRFINPMLKHQYG--VDSMPETAENVAEDFQISRAD 182

Query: 167 QDEYSLESQRRTAAAQQGGKFNDEIAPISTKMGVVDKATGAVSFKDITLSQDEGPRPETT 226
           QD ++L SQ R A AQ  G    EI  ++      D            + +DE PRPETT
Sbjct: 183 QDAFALRSQERAARAQADGILAQEITAVAIPTRQGDHRR---------VDRDEHPRPETT 233

Query: 227 AEGLAGLKA-VRGEGFTITAGNASQLSDGASATVIMSDKTAAAKGLKPLGIFRGMVSYGC 285
           AEGLA LK  VR +G T+TAGNAS ++DGA+A V+ S + AA  GL PL    G+ S G 
Sbjct: 234 AEGLAKLKPFVRRDG-TVTAGNASGVNDGAAALVLASAEAAARHGLTPLTRVLGLASAGV 292

Query: 286 EPDEMGIGPVFAVPRLLKRHGLSVDDIGLWELNEAFAVQVLYCRDKLGI--DPEKLNVNG 343
            P  MGIGPV AV  L  R GL   D  + ELNEAFA Q L C   LG+  D E +N +G
Sbjct: 293 PPRVMGIGPVPAVTALCARLGLKPSDFDVIELNEAFASQSLACLRGLGLPDDAEHVNPHG 352

Query: 344 GAISVGHPYGMSGARLAGHALIEGRRRKAKYAVVTMCVGGGMGSA 388
           GAI+ GHP GMSGAR+AG A  E  RR  +  + T+CVG G G A
Sbjct: 353 GAIAFGHPLGMSGARIAGAATRELVRRGGRLGLATLCVGVGQGVA 397


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: 425
Number of extensions: 23
Number of successful extensions: 4
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: 404
Length adjustment: 31
Effective length of query: 364
Effective length of database: 373
Effective search space:   135772
Effective search space used:   135772
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 Apr 09 2024. 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