GapMind for catabolism of small carbon sources

 

Alignments for a candidate for D-LDH in Oceanisphaera arctica V1-41

Align D-lactate dehydrogenase (EC 1.1.1.28) (characterized)
to candidate WP_104487446.1 UN63_RS13580 D-2-hydroxyacid dehydrogenase

Query= BRENDA::Q9I530
         (329 letters)



>NCBI__GCF_002936955.1:WP_104487446.1
          Length = 316

 Score =  160 bits (406), Expect = 3e-44
 Identities = 111/336 (33%), Positives = 175/336 (52%), Gaps = 30/336 (8%)

Query: 1   MRILFFSSQAYDSE-SFQASNHRHGFELHFQQAHLQADTAVLAQGFEVVCAFVND-DLSR 58
           M+++F   +    E   +A +  H +E H + A  Q    VL +  +   A VN   L  
Sbjct: 1   MKLVFLDRKTLAPEIELRAPSFPHRWEEHEETAPHQ----VLERLQDTDIAIVNKVRLGA 56

Query: 59  PVLERLAAGGTRLVALRSAGYNHVDLAAAEALGLPVVHVPAYSPHAVAEHAVGLILTLNR 118
            +L RL     +LV + + G ++VDL A    G+ V ++  YS ++V EHA+ LIL LNR
Sbjct: 57  DILSRLPR--LKLVVIAATGSDNVDLEACRQAGIAVCNIRDYSKNSVPEHALALILALNR 114

Query: 119 RLHRAYNRT-------REGDFSLHGLTGFDLHGKRVGVIGTGQIGETFARIMAGFGCELL 171
            L+ AY  +       + G F        DL G+ +G+IG G I     ++    G +++
Sbjct: 115 SLN-AYRASIVAGRWQQSGQFCYFDYPVRDLAGQTLGLIGYGTIARELEKLATALGMKVI 173

Query: 172 AYDPYPNPRIQALGGRYLALDALLAESDIVSLHCPLTADTRHLIDAQRLATMKPGAMLIN 231
                 +P  +   G     + LL ++D++SLHCPL A+TRHLI  + L  MK  A+L+N
Sbjct: 174 VAARKGHPVSEGRVG----FEQLLNDADVISLHCPLNAETRHLIGERELKLMKSDALLVN 229

Query: 232 TGRGALVNAAALIEALKSGQLGYLGLDVYEEEADIFFEDRSDQPLQDDVLARLLSFPNVV 291
            GRG LV+ AAL+ AL+  ++G  G DV  +E           P  D+ L + L +PN +
Sbjct: 230 VGRGGLVDEAALLAALEQNRIGGAGFDVVTQE----------PPAPDNPLMQALQYPNFI 279

Query: 292 VTAHQAFLTREALAAIADTTLDNIAAWQDGTPRNRV 327
           +T H A+ +R A+  +AD  +DNI A+  G P++R+
Sbjct: 280 LTPHIAWASRNAMQRLADQLIDNIEAFVAGQPQHRL 315


Lambda     K      H
   0.323    0.137    0.402 

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: 280
Number of extensions: 19
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: 329
Length of database: 316
Length adjustment: 28
Effective length of query: 301
Effective length of database: 288
Effective search space:    86688
Effective search space used:    86688
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.5 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (22.0 bits)
S2: 48 (23.1 bits)

This GapMind analysis is from Sep 24 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