GapMind for catabolism of small carbon sources

 

Alignments for a candidate for ARO8 in Caulobacter crescentus NA1000

Align aspartate transaminase (EC 2.6.1.1) (characterized)
to candidate CCNA_01446 CCNA_01446 LL-diaminopimelate aminotransferase

Query= BRENDA::Q8YTF2
         (403 letters)



>FitnessBrowser__Caulo:CCNA_01446
          Length = 406

 Score =  335 bits (860), Expect = 1e-96
 Identities = 168/386 (43%), Positives = 246/386 (63%), Gaps = 5/386 (1%)

Query: 7   TPADRIQQLPPYVFARLDELKAKAREQGIDLIDLGMGNPDGATPQPVVDAAIQALQDPKN 66
           T   RI++LPPYVF  ++++KA+ R +G D+ID GMGNPD  TPQ +VD  I+  +DPK 
Sbjct: 3   TDFHRIRRLPPYVFEEVNKIKARLRAEGTDIIDFGMGNPDMPTPQHIVDKLIETARDPKA 62

Query: 67  HGYPPFEGTASFRRAITNWYNRRYGVVLDPDSEALPLLGSKEGLSHLAIAYVNPGDVVLV 126
             Y   +G    R+A+ N+Y RR+GV L+PD+E +  LGSKEG ++LA A   PGDV++ 
Sbjct: 63  GRYSASKGVPGLRKAMANYYGRRFGVKLNPDTEVIATLGSKEGFANLAQALTGPGDVIIC 122

Query: 127 PSPAYPAHFRGPVIAGGTV-HSLILKPENDWLIDLTAIPEEVARKAKILYFNYPSNPTGA 185
           P+PAYP H  G ++AGG + H   L PE ++L +++   +       +L  +YPSNPT  
Sbjct: 123 PNPAYPIHAFGFIMAGGIIRHVPALSPE-EYLSNISRAVKHSVPPPSVLILSYPSNPTAQ 181

Query: 186 TAPREFFEEIVAFARKYEILLVHDLCYAELAFDGYQPTSLLEIPGAKDIGVEFHTLSKTY 245
               +F+++ VA A+K+++L++ D+ Y E+ FD   P S+L++ GAKDI VE ++LSKTY
Sbjct: 182 WVDLDFYKDAVALAKKHDLLVISDVAYGEIYFDNNPPPSILQVDGAKDIAVEVNSLSKTY 241

Query: 246 NMAGWRVGFVVGNRHVIQGLRTLKTNLDYGIFAALQTAAETALQLPDIYLHEVQQRYRTR 305
            MAGWRVG VVGN  +   L  +K+ LDYG +  +Q AA TAL  P   + E++  Y++R
Sbjct: 242 AMAGWRVGMVVGNARICAALARVKSYLDYGAYTPVQVAAATALNGPQDCVDEIRGIYKSR 301

Query: 306 RDFLIQGLGELGWDVPKTKATMYLWVKCPVG---MGSTDFALNLLQQTGVVVTPGNAFGV 362
           RD LI+ +   GWD+P   A+M+ W K P      GS  F+  L+++ GV V PG  FG 
Sbjct: 302 RDTLIKSMKAAGWDIPNPPASMFAWAKIPEAYREAGSMLFSRLLIEEAGVAVAPGIGFGE 361

Query: 363 AGEGYVRISLIADCDRLGEALDRIKQ 388
            GEGYVRI L+ +  R+ +A   +K+
Sbjct: 362 YGEGYVRIGLVENEHRIRQAARNVKK 387


Lambda     K      H
   0.321    0.140    0.427 

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: 486
Number of extensions: 13
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: 403
Length of database: 406
Length adjustment: 31
Effective length of query: 372
Effective length of database: 375
Effective search space:   139500
Effective search space used:   139500
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