GapMind for catabolism of small carbon sources

 

Alignments for a candidate for ltaE in Marinobacter adhaerens HP15

Align Serine hydroxymethyltransferase; SHMT; Serine methylase; EC 2.1.2.1; L-threonine/L-allo-threonine aldolase; EC 4.1.2.48 (uncharacterized)
to candidate GFF502 HP15_489 glycine hydroxymethyltransferase

Query= curated2:D3DKC4
         (427 letters)



>FitnessBrowser__Marino:GFF502
          Length = 417

 Score =  516 bits (1328), Expect = e-151
 Identities = 253/405 (62%), Positives = 316/405 (78%), Gaps = 2/405 (0%)

Query: 8   DAEIYEAIVKEYERQFYHLELIASENFTSLAVMEAQGSVMTNKYAEGLPHKRYYGGCEFV 67
           D E++ A+  E +RQ  H+ELIASEN+TS  VMEAQGSV+TNKYAEG P KRYYGGCEFV
Sbjct: 12  DDELWNAMQAEEKRQEAHIELIASENYTSPRVMEAQGSVLTNKYAEGYPGKRYYGGCEFV 71

Query: 68  DIAEDLAIERAKALFDAEHANVQPHSGTQANMAVYMAVLKPGDTIMGMDLSHGGHLTHGA 127
           DIAE+LAIERAK LF A +ANVQPHSG+QAN AV+MA+LKPGDT++GM L+HGGHLTHGA
Sbjct: 72  DIAEELAIERAKELFGAAYANVQPHSGSQANSAVFMALLKPGDTVLGMSLAHGGHLTHGA 131

Query: 128 KVNFSGKIYNAVYYGVHPETHLIDYDQLYRLAKEHKPKLIVGGASAYPRVIDWAKLREIA 187
            VNFSGKIYNAV YG++ +T L+DYD++  LA EHKPK+I+ G SAY + +D+A+ REIA
Sbjct: 132 SVNFSGKIYNAVQYGINTDTGLLDYDEIESLALEHKPKMIIAGFSAYSQELDFARFREIA 191

Query: 188 DSVGAYLMVDMAHYAGLIAGGVYPNPVPYAHFVTSTTHKTLRGPRSGFILC--KKEFAKD 245
           D VGAYL VDMAH AGL+A GVYP+PVP+AH V +TTHKTLRGPR G IL     +  K 
Sbjct: 192 DKVGAYLFVDMAHVAGLVAAGVYPDPVPHAHVVATTTHKTLRGPRGGLILACDDADLQKK 251

Query: 246 IDKSVFPGIQGGPLMHVIAAKAVAFKEAMSQEFKEYARQVVANARVLAEEFIKEGFKVVS 305
           ++ +VFPG QGGPLMHVIAAKAV FKEAMS +FK Y +QVV NA  +A+ F+  G+ VVS
Sbjct: 252 LNSAVFPGGQGGPLMHVIAAKAVCFKEAMSDDFKTYQQQVVKNASAMAQVFVDRGYDVVS 311

Query: 306 GGTDSHIVLLDLRDTGLTGREVEEALGKANITVNKNAVPFDPLPPVKTSGIRLGTPAMTT 365
           GGT +H+ L+ L    +TG++ + ALG+A+ITVNKNAVP DP  P  TSG+R+GTPA+TT
Sbjct: 312 GGTKNHLFLVSLIKQDITGKDADAALGRAHITVNKNAVPNDPRSPFVTSGLRIGTPAITT 371

Query: 366 RGMKEDQMRIIARLISKVIKNIGDEKVIEYVRQEVIEMCEQFPLY 410
           RG  E + R +A  I  ++ N+ DE V   VR++V  +C +FP+Y
Sbjct: 372 RGFGESECRDLAGWICDILDNLDDEAVNSRVREQVSALCARFPVY 416


Lambda     K      H
   0.319    0.136    0.395 

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: 600
Number of extensions: 34
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: 427
Length of database: 417
Length adjustment: 32
Effective length of query: 395
Effective length of database: 385
Effective search space:   152075
Effective search space used:   152075
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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.

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