GapMind for Amino acid biosynthesis

 

Alignments for a candidate for leuD in Pseudomonas fluorescens GW456-L13

Align 3-isopropylmalate dehydratase small subunit; EC 4.2.1.33 (characterized, see rationale)
to candidate PfGW456L13_3947 3-isopropylmalate dehydratase small subunit (EC 4.2.1.33)

Query= uniprot:Q845W4
         (216 letters)



>FitnessBrowser__pseudo13_GW456_L13:PfGW456L13_3947
          Length = 214

 Score =  320 bits (819), Expect = 2e-92
 Identities = 152/210 (72%), Positives = 173/210 (82%)

Query: 1   MEKFTVHTGVVAPLDRENVDTDAIIPKQFLKSIKRTGFGPNAFDEWRYLDHGEPGQDNSK 60
           M+ FT HTG+VAPLDR NVDTD IIPKQFLKSIKRTGFGPN FDEWRYLD G+P QDNSK
Sbjct: 1   MKAFTQHTGLVAPLDRANVDTDQIIPKQFLKSIKRTGFGPNLFDEWRYLDVGQPYQDNSK 60

Query: 61  RPLNPDFVLNQPRYQGASILVTRKNFGCGSSREHAPWALQQYGFRAIIAPSFADIFFNNC 120
           RPLN DFVLN  RYQGAS+L+ R+NFGCGSSREHAPWAL++YGFR+IIAPS+ADIFFNN 
Sbjct: 61  RPLNKDFVLNAERYQGASVLLARENFGCGSSREHAPWALEEYGFRSIIAPSYADIFFNNS 120

Query: 121 FKNGLLPIVLTEQQVDHLINETVAFNGYQLTIDLEAQVVRTPDGRDYPFEITAFRKYCLL 180
           FKNGLLPI+L++ +VD L  +  A  GYQL +DL+AQ V  PDG+   FEI AFRK+CLL
Sbjct: 121 FKNGLLPIILSDAEVDELFQQVEANPGYQLQVDLQAQTVTRPDGKVLSFEIDAFRKHCLL 180

Query: 181 NGFDDIGLTLRHADKIRQFEAERLAKQPWL 210
           NG DDIGLTL+  D I  FEA+  A QPWL
Sbjct: 181 NGLDDIGLTLQDGDAIAAFEAKHRASQPWL 210


Lambda     K      H
   0.322    0.141    0.437 

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: 230
Number of extensions: 4
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: 216
Length of database: 214
Length adjustment: 22
Effective length of query: 194
Effective length of database: 192
Effective search space:    37248
Effective search space used:    37248
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: 45 (21.9 bits)

Align candidate PfGW456L13_3947 (3-isopropylmalate dehydratase small subunit (EC 4.2.1.33))
to HMM TIGR00171 (leuD: 3-isopropylmalate dehydratase, small subunit (EC 4.2.1.33))

# 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.aa/TIGR00171.hmm
# target sequence database:        /tmp/gapView.20673.genome.faa
# - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - - -

Query:       TIGR00171  [M=188]
Accession:   TIGR00171
Description: leuD: 3-isopropylmalate dehydratase, small subunit
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
    ------- ------ -----    ------- ------ -----   ---- --  --------                                               -----------
    2.7e-94  300.4   0.0    3.4e-94  300.1   0.0    1.1  1  lcl|FitnessBrowser__pseudo13_GW456_L13:PfGW456L13_3947  3-isopropylmalate dehydratase sm


Domain annotation for each sequence (and alignments):
>> lcl|FitnessBrowser__pseudo13_GW456_L13:PfGW456L13_3947  3-isopropylmalate dehydratase small subunit (EC 4.2.1.33)
   #    score  bias  c-Evalue  i-Evalue hmmfrom  hmm to    alifrom  ali to    envfrom  env to     acc
 ---   ------ ----- --------- --------- ------- -------    ------- -------    ------- -------    ----
   1 !  300.1   0.0   3.4e-94   3.4e-94       1     188 []       1     196 [.       1     196 [. 0.94

  Alignments for each domain:
  == domain 1  score: 300.1 bits;  conditional E-value: 3.4e-94
                                               TIGR00171   1 mkefkkltGlvvpldkanvdtdaiipkqflkkikrtGfgkhlfyewryld..... 50 
                                                             mk f ++tGlv+pld+anvdtd+iipkqflk ikrtGfg +lf ewryld     
  lcl|FitnessBrowser__pseudo13_GW456_L13:PfGW456L13_3947   1 MKAFTQHTGLVAPLDRANVDTDQIIPKQFLKSIKRTGFGPNLFDEWRYLDvgqpy 55 
                                                             899*********************************************9833332 PP

                                               TIGR00171  51 .ekGkep.npefvlnvpqyqgasillarenfGcGssrehapwalkdyGfkviiap 103
                                                              ++ k p n +fvln ++yqgas+llarenfGcGssrehapwal++yGf++iiap
  lcl|FitnessBrowser__pseudo13_GW456_L13:PfGW456L13_3947  56 qDNSKRPlNKDFVLNAERYQGASVLLARENFGCGSSREHAPWALEEYGFRSIIAP 110
                                                             2233333489********************************************* PP

                                               TIGR00171 104 sfadifynnsfkngllpirlseeeveellalvk.nkglkltvdleaqkvkdsegk 157
                                                             s+adif+nnsfkngllpi ls++ev+el+++v+ n+g +l+vdl+aq+v+  +gk
  lcl|FitnessBrowser__pseudo13_GW456_L13:PfGW456L13_3947 111 SYADIFFNNSFKNGLLPIILSDAEVDELFQQVEaNPGYQLQVDLQAQTVTRPDGK 165
                                                             ********************************99********************* PP

                                               TIGR00171 158 vysfeidefrkhcllnGldeigltlqkedei 188
                                                             v sfeid+frkhcllnGld+igltlq  d+i
  lcl|FitnessBrowser__pseudo13_GW456_L13:PfGW456L13_3947 166 VLSFEIDAFRKHCLLNGLDDIGLTLQDGDAI 196
                                                             **************************99987 PP



Internal pipeline statistics summary:
-------------------------------------
Query model(s):                            1  (188 nodes)
Target sequences:                          1  (214 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: 0.00u 0.01s 00:00:00.01 Elapsed: 00:00:00.00
# Mc/sec: 5.43
//
[ok]

This GapMind analysis is from Apr 09 2024. The underlying query database was built on Apr 09 2024.

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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