GapMind for catabolism of small carbon sources

 

Alignments for a candidate for andAc in Cupriavidus basilensis 4G11

Align Anthranilate 1,2-dioxygenase large subunit; EC 1.14.12.1 (characterized)
to candidate RR42_RS26425 RR42_RS26425 biphenyl 2,3-dioxygenase

Query= SwissProt::Q84BZ3
         (423 letters)



>FitnessBrowser__Cup4G11:RR42_RS26425
          Length = 429

 Score =  360 bits (924), Expect = e-104
 Identities = 179/407 (43%), Positives = 261/407 (64%), Gaps = 5/407 (1%)

Query: 21  FPHDDGSRVPYKVFSSRAVYDREQERIFRGPTWNFVALEAEIPNAGDFKSTFVGDTPVVV 80
           +P D    +P  V++S AVYD E E+IFRG +WNFVALEAEIPN GDFK ++VG TPVVV
Sbjct: 24  WPEDALHFIPDWVYTSNAVYDLELEKIFRGRSWNFVALEAEIPNPGDFKRSYVGPTPVVV 83

Query: 81  TRTEDGALSAWVNRCAHRGAQVCRKSRGNASSHTCVYHQWSFDNEGNLLGVPFRRGQKGM 140
            R EDG+++ + NRCAHRGA+ CR  +GNA    C YHQWS+D +GNL GVPF+RG    
Sbjct: 84  ARAEDGSVNVFENRCAHRGAEFCRHGQGNAKEFVCPYHQWSYDLKGNLQGVPFKRGVNRA 143

Query: 141 TGMPADFDPKQHGLRKLRVDSYRGLVFATFSDDVAPLPDYLGAQMRPWIDRIFH-KPIEY 199
            GMP DF  + HGL KL V +  G++FA++++D+ PL  Y+  ++    D +F+ KP++ 
Sbjct: 144 GGMPKDFRNEDHGLVKLNVATRNGVIFASYANDMEPLDVYMTPEILKDFDVVFNGKPLKI 203

Query: 200 LGCTRQYSKSNWKLYMENVKDPYHASMLHLFHTTFNIFRVGMKARSIPDANHGLHSIITV 259
           LG  +     NWK+Y EN+KDPYHA++LH F   F +   G  +  I D  HG H  +  
Sbjct: 204 LGYYKNELPCNWKMYHENLKDPYHATLLHSFLVVFGLLVAGNDSAMIADPVHGRHGTMAS 263

Query: 260 TKTGDDTSAAYKQQN---IRSFDEGFHLEDESILDLVSEYDEDCTNHIQPIFPQLVIQQI 316
            K  +D  AA   +N   +RS+ EG  L+D+  L+ + E+D   +  +Q I+P L++Q+ 
Sbjct: 264 AKK-EDKYAAVSDENKKEMRSYHEGMRLQDDRFLEYIKEFDSPWSVTMQTIWPNLIVQRE 322

Query: 317 HNTLVARQILPKGPDNFELIFHFFGYADDTPELRALRIKQANLVGPAGYISMEDTEATEL 376
            NTL  RQI+P GPD+  + +  FGY DDT E+   R++Q NL+GPAG++ +ED EA + 
Sbjct: 323 MNTLGVRQIVPNGPDSMLMQWTMFGYEDDTEEMTRHRLRQGNLMGPAGFLGLEDNEAMKF 382

Query: 377 VQRGTVRDADATSVIEMSRGNPEQQDTVITESLIRKFWVGYQKLMGY 423
           VQ G  R +   +V+++  G+    +++I+ES IR  +  Y+ +MG+
Sbjct: 383 VQEGVRRSSTERNVLKLDPGHVGTANSLISESAIRAMYQYYRSVMGF 429


Lambda     K      H
   0.321    0.136    0.420 

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: 574
Number of extensions: 30
Number of successful extensions: 3
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: 423
Length of database: 429
Length adjustment: 32
Effective length of query: 391
Effective length of database: 397
Effective search space:   155227
Effective search space used:   155227
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: 51 (24.3 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