GapMind for catabolism of small carbon sources

 

Alignments for a candidate for mt2d in Herbaspirillum seropedicae SmR1

Align mannitol 2-dehydrogenase (EC 1.1.1.67) (characterized)
to candidate HSERO_RS17015 HSERO_RS17015 sulfurtransferase

Query= BRENDA::Q8KQG6
         (338 letters)



>FitnessBrowser__HerbieS:HSERO_RS17015
          Length = 345

 Score =  130 bits (326), Expect = 6e-35
 Identities = 102/333 (30%), Positives = 159/333 (47%), Gaps = 35/333 (10%)

Query: 1   MEALVLTGTKKLEVKDIDRPKVL-PNEVLIHTAFAGICGTDHALYA-GLPGSADAVPPIV 58
           M+ALVL  T++L++++ID P+ +   +V I     GICG+D   Y  G  G      P+V
Sbjct: 1   MQALVLEATRELKLREIDLPQQMGAQDVRIRIHTVGICGSDLHYYTHGSIGPFKVEAPMV 60

Query: 59  LGHENSGVVAEIGSAVTNVKVGDRVTVDPNIYCGQCKYCRTARPELCENLSAVGVTRDGG 118
           LGHE SG V E+GSAV+++KVGDRV ++P I            P L    +  G+     
Sbjct: 61  LGHEASGTVIEVGSAVSHLKVGDRVCMEPGI------------PRLDSPATLRGMYNLDP 108

Query: 119 FEEFFTAP-------ASVVYP------IPDNVSLKSAAVVEPISCAVHGIQLLKVTPYQK 165
              F+  P        SVV+P      +PDNVS    A+VEP+S  +      ++ P   
Sbjct: 109 AVRFWATPPIHGCLTGSVVHPAAFTYRLPDNVSFAEGAIVEPLSIGLQAATKARMKPGDT 168

Query: 166 ALVIGDGFMGELFVQILQAYGIHQVDLAGIVDEKLAMNKEKFGV------KNTYNTMKGD 219
           A+VIG G +G +      A G  +V LA +V EKLA   +   V      + T   +   
Sbjct: 169 AVVIGAGTIGAMTALAALAGGAARVILADVVAEKLAHFADNPAVITVDVTRETLTDVVRQ 228

Query: 220 KIPEGEYDVIIEAVGLPQTQEAAIEASARGAQVLMFGVGGPDAKFQMNTYEVFQKQLTIQ 279
                  DV+ EA G     +  ++    G   ++  VG P A   ++   +  K++ ++
Sbjct: 229 ATDGWGADVVFEASGHAGVYQTLLDLVCPGGCAVL--VGMPPAPVALDVVAMQTKEVRLE 286

Query: 280 GSFINPNAFEDSLALLSSGKLNVEALMSHELDY 312
             F   N F  +LAL+SSG ++V+  +S +  +
Sbjct: 287 SVFRYANIFPRALALISSGMIDVKPFISRKFPF 319


Lambda     K      H
   0.317    0.136    0.390 

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: 268
Number of extensions: 11
Number of successful extensions: 4
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 1
Length of query: 338
Length of database: 345
Length adjustment: 29
Effective length of query: 309
Effective length of database: 316
Effective search space:    97644
Effective search space used:    97644
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: 49 (23.5 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