GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gloB in Cupriavidus basilensis 4G11

Align hydroxyacylglutathione hydrolase (EC 3.1.2.6) (characterized)
to candidate RR42_RS13570 RR42_RS13570 hydroxyacylglutathione hydrolase

Query= BRENDA::Q8ZRM2
         (251 letters)



>FitnessBrowser__Cup4G11:RR42_RS13570
          Length = 267

 Score =  183 bits (464), Expect = 4e-51
 Identities = 109/268 (40%), Positives = 148/268 (55%), Gaps = 20/268 (7%)

Query: 1   MNLNSIPAFQDNYIWVLTNDEGRCV-IVDPGEAAPVLKAIAEHKWMPEAIFLTHHHHDHV 59
           + +  IPAFQDNYIW +   +G C  +VDPGE+APV   +A       AI +THHH DH 
Sbjct: 2   LKVEPIPAFQDNYIWAI--HDGHCAAVVDPGESAPVEAFLAREGLTLGAIVITHHHGDHQ 59

Query: 60  GGVKELLQHFPQ------MTVYGPAETQDKGATHLVGDGDTIRVLGEKFTL--FATPGHT 111
           GGV  LL   P       + V GPA  +    T  V +GDT+ V      L     PGHT
Sbjct: 60  GGVAGLLAVHPTAPDGAPLPVIGPAGERIGARTVAVREGDTVNVAHPSLQLKVLDVPGHT 119

Query: 112 LGHVCYFSR-----PYLFCGDTLFSGGCGRLFEGTPSQMYQSLMKINSLPDDTLICCAHE 166
            GHV Y +      P +FCGDTLF+ GCGRLFEG+P+QM  SL K+ +LP  T + CAHE
Sbjct: 120 AGHVAYVADLPGAGPSVFCGDTLFASGCGRLFEGSPAQMLSSLDKLAALPGATRVYCAHE 179

Query: 167 YTLANIKFALSILPHDSFINEYYRKVKELRVKKQMTLPVILKNERKINLFLRTEDIDLIN 226
           YT +N++FA ++ PH++ +  +  +V  LR     T+P  +  ER++N FLR+  +  + 
Sbjct: 180 YTRSNVRFARAVEPHNAELAAWEARVDALRAVGAPTVPTTIGQEREVNPFLRSR-VPAVR 238

Query: 227 E---INKETILQQPEARFAWLRSKKDTF 251
           E    +   +     A F  LR  KD F
Sbjct: 239 EAVAAHAGGVAGNDAAAFGALRGWKDDF 266


Lambda     K      H
   0.323    0.140    0.436 

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: 209
Number of extensions: 9
Number of successful extensions: 5
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: 251
Length of database: 267
Length adjustment: 24
Effective length of query: 227
Effective length of database: 243
Effective search space:    55161
Effective search space used:    55161
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 (21.9 bits)
S2: 47 (22.7 bits)

Align candidate RR42_RS13570 RR42_RS13570 (hydroxyacylglutathione hydrolase)
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.29458.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
    ------- ------ -----    ------- ------ -----   ---- --  --------                                 -----------
    1.7e-95  305.1   0.0    1.9e-95  304.9   0.0    1.0  1  lcl|FitnessBrowser__Cup4G11:RR42_RS13570  RR42_RS13570 hydroxyacylglutathi


Domain annotation for each sequence (and alignments):
>> lcl|FitnessBrowser__Cup4G11:RR42_RS13570  RR42_RS13570 hydroxyacylglutathione hydrolase
   #    score  bias  c-Evalue  i-Evalue hmmfrom  hmm to    alifrom  ali to    envfrom  env to     acc
 ---   ------ ----- --------- --------- ------- -------    ------- -------    ------- -------    ----
   1 !  304.9   0.0   1.9e-95   1.9e-95       2     248 .]       5     266 ..       4     266 .. 0.94

  Alignments for each domain:
  == domain 1  score: 304.9 bits;  conditional E-value: 1.9e-95
                                 TIGR03413   2 iaipalsdNyiwllkdekseavvvDpgeaepvlealeekglkleaillTHhHaDHvggvaellekfp.. 68 
                                               ++ipa++dNyiw+++d +  a+vvDpge++pv ++l+++gl+l ai++THhH DH ggva ll+ +p  
  lcl|FitnessBrowser__Cup4G11:RR42_RS13570   5 EPIPAFQDNYIWAIHDGH-CAAVVDPGESAPVEAFLAREGLTLGAIVITHHHGDHQGGVAGLLAVHPta 72 
                                               78****************.99*****************************************9876532 PP

                                 TIGR03413  69 .....vkvvgpaeeripgltkevkegdevel..lelevevlevpGHtlgHiayyleee...kvlFcgDt 127
                                                    ++v+gpa eri + t++v+egd+v++   +l+++vl+vpGHt+gH+ay+++     + +FcgDt
  lcl|FitnessBrowser__Cup4G11:RR42_RS13570  73 pdgapLPVIGPAGERIGARTVAVREGDTVNVahPSLQLKVLDVPGHTAGHVAYVADLPgagPSVFCGDT 141
                                               2333478***********************955578999***************99656779******* PP

                                 TIGR03413 128 LfsaGCGrlfegtaeqmleslqklaaLpeetkvycaHEYtlsNlrFalavepenealkerlkevealra 196
                                               Lf+ GCGrlfeg+++qml+sl+klaaLp +t+vycaHEYt sN+rFa+avep+n++l+++ ++v+alra
  lcl|FitnessBrowser__Cup4G11:RR42_RS13570 142 LFASGCGRLFEGSPAQMLSSLDKLAALPGATRVYCAHEYTRSNVRFARAVEPHNAELAAWEARVDALRA 210
                                               ********************************************************************* PP

                                 TIGR03413 197 kgkptlPstlaeekatNpFLraeeaevkaalee....ekaeevevfaelRekkdkf 248
                                                g pt+P+t+++e+++NpFLr + ++v++a+++     + +++++f +lR +kd+f
  lcl|FitnessBrowser__Cup4G11:RR42_RS13570 211 VGAPTVPTTIGQEREVNPFLRSRVPAVREAVAAhaggVAGNDAAAFGALRGWKDDF 266
                                               *****************************9999888888999************98 PP



Internal pipeline statistics summary:
-------------------------------------
Query model(s):                            1  (248 nodes)
Target sequences:                          1  (267 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 0.01s 00:00:00.02 Elapsed: 00:00:00.01
# Mc/sec: 5.96
//
[ok]

This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.

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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