GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gloB in Sinorhizobium meliloti 1021

Align Hydroxyacylglutathione hydrolase; EC 3.1.2.6; Glyoxalase II; Glx II (uncharacterized)
to candidate SMc00708 SMc00708 hydroxyacylglutathione hydrolase (glyoxalase II) (GLX II) protein

Query= curated2:Q8U9W1
         (256 letters)



>FitnessBrowser__Smeli:SMc00708
          Length = 256

 Score =  352 bits (902), Expect = e-102
 Identities = 167/256 (65%), Positives = 200/256 (78%)

Query: 1   MKPLEIDVFLCRSDNFGVLLHDPESGATAAIDAPEEGPILRALDGHGWKLTHIFTTHHHQ 60
           M  LE+D+FLCR+DN+GVLLHD  SGATA+IDAPEE PIL AL+  GW+LTHI TTHHH 
Sbjct: 1   MAALELDLFLCRTDNYGVLLHDRLSGATASIDAPEERPILDALERRGWQLTHILTTHHHG 60

Query: 61  DHVEANLVLKDKFRCEVHGPYDEAIAIPGLDRSQADGDEFEFAGRRVQVIATPGHTAGHI 120
           DHV AN  LK++F   + GP +EA  IPG+DR+   GD F+FAG  V VI TPGHT+GH+
Sbjct: 61  DHVAANASLKERFGLTIIGPKNEASKIPGIDRTVGHGDRFDFAGHPVDVIETPGHTSGHV 120

Query: 121 CYYLPDDGLLFAADTLFAMGCGRLFERPAADMWHSFQKLMALPDDTRVYFGHEYTLSNAR 180
           CY+LP+D LLFAADTLFA+GCGRLFE  A  MW S  +LMALPDDT +YFGHEYTL+NA 
Sbjct: 121 CYHLPEDKLLFAADTLFALGCGRLFEGTADTMWQSLSRLMALPDDTAIYFGHEYTLANAH 180

Query: 181 FALTVDPDNAVLRERAARVETARQANEFTIPTTIGLEKQTNPYMRVADAGIRRHLGLEGA 240
           FA+TVDP+N+ L+ERAA +E  R    FT PTT+GLEK+TNP++R  D  IR  LG+E A
Sbjct: 181 FAITVDPENSALKERAAEIEETRSDGGFTAPTTMGLEKRTNPFLRAGDPKIRALLGMEKA 240

Query: 241 ADADVFAEIRTRKDNF 256
           +DA VFAEIR RKDNF
Sbjct: 241 SDAAVFAEIRKRKDNF 256


Lambda     K      H
   0.323    0.139    0.430 

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: 307
Number of extensions: 5
Number of successful extensions: 1
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: 256
Length of database: 256
Length adjustment: 24
Effective length of query: 232
Effective length of database: 232
Effective search space:    53824
Effective search space used:    53824
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: 47 (22.7 bits)

Align candidate SMc00708 SMc00708 (hydroxyacylglutathione hydrolase (glyoxalase II) (GLX II) protein)
to HMM TIGR03413 (gloB: hydroxyacylglutathione hydrolase (EC 3.1.2.6))

# hmmsearch :: search profile(s) against a sequence database
# HMMER 3.3.1 (Jul 2020); http://hmmer.org/
# Copyright (C) 2020 Howard Hughes Medical Institute.
# Freely distributed under the BSD open source license.
# - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - -
# query HMM file:                  ../tmp/path.carbon/TIGR03413.hmm
# target sequence database:        /tmp/gapView.3583.genome.faa
# - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - -

Query:       TIGR03413  [M=248]
Accession:   TIGR03413
Description: GSH_gloB: hydroxyacylglutathione hydrolase
Scores for complete sequences (score includes all domains):
   --- full sequence ---   --- best 1 domain ---    -#dom-
    E-value  score  bias    E-value  score  bias    exp  N  Sequence                           Description
    ------- ------ -----    ------- ------ -----   ---- --  --------                           -----------
   2.3e-100  321.1   0.0   2.5e-100  320.9   0.0    1.0  1  lcl|FitnessBrowser__Smeli:SMc00708  SMc00708 hydroxyacylglutathione 


Domain annotation for each sequence (and alignments):
>> lcl|FitnessBrowser__Smeli:SMc00708  SMc00708 hydroxyacylglutathione hydrolase (glyoxalase II) (GLX II) protein
   #    score  bias  c-Evalue  i-Evalue hmmfrom  hmm to    alifrom  ali to    envfrom  env to     acc
 ---   ------ ----- --------- --------- ------- -------    ------- -------    ------- -------    ----
   1 !  320.9   0.0  2.5e-100  2.5e-100       5     248 .]      10     256 .]       6     256 .] 0.99

  Alignments for each domain:
  == domain 1  score: 320.9 bits;  conditional E-value: 2.5e-100
                           TIGR03413   5 palsdNyiwllkdeks.eavvvDpgeaepvlealeekglkleaillTHhHaDHvggvaellekfpvkvvgpaee. 77 
                                          + +dNy +ll+d+ s +++ +D++e++p+l+ale++g++l++il+THhH DHv ++a+l+e+f+++++gp++e 
  lcl|FitnessBrowser__Smeli:SMc00708  10 LCRTDNYGVLLHDRLSgATASIDAPEERPILDALERRGWQLTHILTTHHHGDHVAANASLKERFGLTIIGPKNEa 84 
                                         6889**********999********************************************************99 PP

                           TIGR03413  78 .ripgltkevkegdevellelevevlevpGHtlgHiayyleeekvlFcgDtLfsaGCGrlfegtaeqmleslqkl 151
                                          +ipg++++v +gd+++++++ v+v+e+pGHt+gH++y+l+e+k+lF++DtLf++GCGrlfegta++m++sl++l
  lcl|FitnessBrowser__Smeli:SMc00708  85 sKIPGIDRTVGHGDRFDFAGHPVDVIETPGHTSGHVCYHLPEDKLLFAADTLFALGCGRLFEGTADTMWQSLSRL 159
                                         9************************************************************************** PP

                           TIGR03413 152 aaLpeetkvycaHEYtlsNlrFalavepenealkerlkevealrakgkptlPstlaeekatNpFLraeeaevkaa 226
                                          aLp++t++y +HEYtl+N++Fa++v+pen+alker++e+e++r++g  t P+t++ ek+tNpFLra +++++a 
  lcl|FitnessBrowser__Smeli:SMc00708 160 MALPDDTAIYFGHEYTLANAHFAITVDPENSALKERAAEIEETRSDGGFTAPTTMGLEKRTNPFLRAGDPKIRAL 234
                                         *************************************************************************** PP

                           TIGR03413 227 leeekaeevevfaelRekkdkf 248
                                         l++eka++++vfae+R++kd+f
  lcl|FitnessBrowser__Smeli:SMc00708 235 LGMEKASDAAVFAEIRKRKDNF 256
                                         ********************98 PP



Internal pipeline statistics summary:
-------------------------------------
Query model(s):                            1  (248 nodes)
Target sequences:                          1  (256 residues searched)
Passed MSV filter:                         1  (1); expected 0.0 (0.02)
Passed bias filter:                        1  (1); expected 0.0 (0.02)
Passed Vit filter:                         1  (1); expected 0.0 (0.001)
Passed Fwd filter:                         1  (1); expected 0.0 (1e-05)
Initial search space (Z):                  1  [actual number of targets]
Domain search space  (domZ):               1  [number of targets reported over threshold]
# CPU time: 0.01u 0.00s 00:00:00.01 Elapsed: 00:00:00.00
# Mc/sec: 6.78
//
[ok]

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