GapMind for catabolism of small carbon sources

 

Alignments for a candidate for ltaE in Cupriavidus basilensis 4G11

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 RR42_RS15485 RR42_RS15485 serine hydroxymethyltransferase

Query= curated2:D3DKC4
         (427 letters)



>FitnessBrowser__Cup4G11:RR42_RS15485
          Length = 415

 Score =  498 bits (1282), Expect = e-145
 Identities = 250/403 (62%), Positives = 311/403 (77%), Gaps = 1/403 (0%)

Query: 8   DAEIYEAIVKEYERQFYHLELIASENFTSLAVMEAQGSVMTNKYAEGLPHKRYYGGCEFV 67
           D E++ AI KE +RQ  H+ELIASEN+TS AVM AQGS +TNKYAEG P KRYYGGCE+V
Sbjct: 13  DPELFAAIQKEDQRQEEHIELIASENYTSPAVMAAQGSQLTNKYAEGYPGKRYYGGCEYV 72

Query: 68  DIAEDLAIERAKALFDAEHANVQPHSGTQANMAVYMAVLKPGDTIMGMDLSHGGHLTHGA 127
           DI E LAI+R K LF AE ANVQP+SG+QAN  V+ A LKPGDTIMGM L+ GGHLTHG 
Sbjct: 73  DIVEQLAIDRVKQLFGAEAANVQPNSGSQANQGVFFAALKPGDTIMGMSLAEGGHLTHGM 132

Query: 128 KVNFSGKIYNAVYYGVHPETHLIDYDQLYRLAKEHKPKLIVGGASAYPRVIDWAKLREIA 187
            +N SGK +N V YG+      IDYD L +LA+E KPKLI+ GASA+   ID+ ++ ++A
Sbjct: 133 ALNMSGKWFNVVSYGLDANED-IDYDALEKLAQEKKPKLIIAGASAFALRIDFERISKVA 191

Query: 188 DSVGAYLMVDMAHYAGLIAGGVYPNPVPYAHFVTSTTHKTLRGPRSGFILCKKEFAKDID 247
            S+GA  MVDMAHYAGLIA G YPNPVP+A FVT+TTHK+LRGPR G IL K E  K I+
Sbjct: 192 KSIGALFMVDMAHYAGLIAAGEYPNPVPHADFVTTTTHKSLRGPRGGVILMKAEHEKAIN 251

Query: 248 KSVFPGIQGGPLMHVIAAKAVAFKEAMSQEFKEYARQVVANARVLAEEFIKEGFKVVSGG 307
            ++FPGIQGGPLMHVIA KAVAFKEA+S EFK Y +QVV NARVLAE  I+ G ++VSG 
Sbjct: 252 SAIFPGIQGGPLMHVIAGKAVAFKEALSPEFKTYQQQVVKNARVLAETLIERGLRIVSGR 311

Query: 308 TDSHIVLLDLRDTGLTGREVEEALGKANITVNKNAVPFDPLPPVKTSGIRLGTPAMTTRG 367
           T+SH++L+DLR   +TG+E E+ LG+A+ITVNKNA+P DP  P  TSGIRLG+PAMTTRG
Sbjct: 312 TESHVMLVDLRAMQITGKEAEKVLGEAHITVNKNAIPNDPEKPFVTSGIRLGSPAMTTRG 371

Query: 368 MKEDQMRIIARLISKVIKNIGDEKVIEYVRQEVIEMCEQFPLY 410
            KE++ R++A L++ V++N  D   I  VR++V  + ++FP+Y
Sbjct: 372 FKEEEARLVANLVADVLENPHDLANIARVREQVAALTKRFPVY 414


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: 540
Number of extensions: 23
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: 427
Length of database: 415
Length adjustment: 32
Effective length of query: 395
Effective length of database: 383
Effective search space:   151285
Effective search space used:   151285
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:

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