GapMind for catabolism of small carbon sources

 

Alignments for a candidate for andAa in Sinorhizobium meliloti 1021

Align Anthranilate 1,2-dioxygenase system ferredoxin--NAD(+) reductase component; EC 1.18.1.3 (characterized)
to candidate SM_b20820 SM_b20820 ferredoxin reductase

Query= SwissProt::Q84BZ0
         (406 letters)



>FitnessBrowser__Smeli:SM_b20820
          Length = 409

 Score =  296 bits (759), Expect = 6e-85
 Identities = 178/410 (43%), Positives = 238/410 (58%), Gaps = 17/410 (4%)

Query: 7   VIVGAGHAARRTAEALRARDADAPIVMIGAERELPYDRPALSKDALLNDDGEQRAFVRDA 66
           VI+GAG    R A ALR +     I + GAE  LPY+RP LSKD L         F+  A
Sbjct: 5   VIIGAGECGARAAFALREKGFGGEITLTGAEPHLPYERPPLSKDGLAQ--ASLPKFIAGA 62

Query: 67  AWYDAQRIALRLGTRVDAIEREAQRVRLDDGTTLPYAKLVLATGSRVRTFGG-PIDAGVV 125
           A Y+  RI +  G   ++I+R  + V L DG +L Y +L+LATG+R R F   P +AG +
Sbjct: 63  ARYEEARITVLTGVTAESIDRVHKAVTLSDGVSLDYDRLLLATGARPRAFPRVPENAGRI 122

Query: 126 AHYVRTVADARALRAQLVRGRRVAVLGGGFIGLEVAAAARQLGCNVTVIDPAARLLQRAL 185
              +RT ADA A+R  L  G R+AV+GGGFIGLE+AA AR+LG  V +++   R+L R +
Sbjct: 123 -RTLRTHADALAIRGALTPGARLAVIGGGFIGLELAATARKLGAEVVLVEGLPRVLSRGV 181

Query: 186 PEVVGAYAHRLHDERGVGFQMATLPRAIRAAAGGGAIVETDRGDVHADVVVVGIGVLPNV 245
           PE +       H   GV         AI  A  G  ++  D  D+ AD++VVGIG +PN 
Sbjct: 182 PEEIAVLVAERHRREGVEIICGAQIAAIDGAGDGARLLLADGVDIEADLIVVGIGAVPNT 241

Query: 246 ELAQAAGLDVDNGIRVDAGCRTAD-----RAIFAAGEVTMHFNPLLGRHVRIESWQVAEN 300
           ELA+AAGL ++NGI VD    T+D     R   AA  +  H+    GR VR+E+W+ A++
Sbjct: 242 ELAEAAGLAIENGIAVDERLCTSDPRHLCRPATAAPSLCPHYG---GRRVRLEAWRNAQD 298

Query: 301 QPAVAAANLLGADDAYAELPWLWSDQYDCNLQMLGLFGAGQTTVVRGDPARGPFTVFGLG 360
           Q A+AAANL+GA +    +PW WSDQY+  LQ+ GL    +TT VR D   G F +F L 
Sbjct: 299 QGALAAANLMGAGETMVSVPWFWSDQYEFTLQIAGLADGAETT-VRRDMEEGAFILFHLD 357

Query: 361 GDGRIVAAAAVNLG----RDIGAARRLIAAGAMPDPQQLADPTVGLKTFL 406
           G+GR++AA+ +  G    RDI  A  LIAAGA P+P  LA P   LK  L
Sbjct: 358 GEGRLIAASGIGPGNAVARDIRLAEMLIAAGAKPEPLALASPETRLKKLL 407


Lambda     K      H
   0.322    0.138    0.410 

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: 370
Number of extensions: 19
Number of successful extensions: 6
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: 406
Length of database: 409
Length adjustment: 31
Effective length of query: 375
Effective length of database: 378
Effective search space:   141750
Effective search space used:   141750
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 (21.9 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