GapMind for catabolism of small carbon sources

 

Alignments for a candidate for glpS in Paraburkholderia bryophila 376MFSha3.1

Align ABC transporter for Glycerol, ATPase component 1 (characterized)
to candidate H281DRAFT_03734 H281DRAFT_03734 carbohydrate ABC transporter ATP-binding protein, CUT1 family

Query= reanno::acidovorax_3H11:Ac3H11_791
         (363 letters)



>FitnessBrowser__Burk376:H281DRAFT_03734
          Length = 364

 Score =  367 bits (943), Expect = e-106
 Identities = 199/357 (55%), Positives = 259/357 (72%), Gaps = 8/357 (2%)

Query: 3   LALDSISKKVGAQTWLYDMSLALQSGAVTVLLGATQAGKTSLMRIMAGLDAPTAGRVTVD 62
           L L+ +S   G Q +LY ++L L  GA+ VLLG TQAGKT+LMR+MAGLD P+AGRV VD
Sbjct: 3   LELEQVSVVSGGQPYLYGVNLRLVPGAINVLLGPTQAGKTTLMRVMAGLDRPSAGRVLVD 62

Query: 63  GKDVTGMPVRDRNVAMVYQQFINYPSMKVAANIASPLKLR--GEKNIDARVREIASRLHI 120
           G+DVTG+ VR RN+AMVYQQFINYP+M V  NIASPL+L+      I  RV+E+A++LHI
Sbjct: 63  GQDVTGVSVRQRNLAMVYQQFINYPAMTVFQNIASPLQLQKTDPAEIRRRVQEVAAKLHI 122

Query: 121 DMFLDRYPAELSGGQQQRVALARALAKGAPLMLLDEPLVNLDYKLREELREELTQLFAAG 180
           +  L+R P+ELSGGQQQR ALARAL K   L+LLDEPLVNLDYKLREELR EL  LFA G
Sbjct: 123 EHLLERRPSELSGGQQQRCALARALVKRTSLVLLDEPLVNLDYKLREELRMELATLFADG 182

Query: 181 QSTVVYATTEPGEALLLGGYTAVLDEGQLLQYGPTAEVFHAPNSLRVARAFSDPPMNLMA 240
           ++TVVYATTEP EALLLGGYTA++D+G++LQ+GPT +V++AP  +  A  F+DPPMN++ 
Sbjct: 183 KTTVVYATTEPLEALLLGGYTAIVDKGRVLQFGPTLDVYNAPVDVDAAAVFNDPPMNMLT 242

Query: 241 ASATAQG-VRLQGGAELTLPLPQGAATAAGLTVGVRASALRVHARPG-DVSVAGVVELAE 298
           +     G  RL  G  + +P+  G A      +G+R   LR+ A+    ++V   +ELAE
Sbjct: 243 SELNGNGSARLPIG--IDVPIHSGTAVNGTCRIGIRPGHLRLAAKTSHSIAVPCRLELAE 300

Query: 299 ISGSDTFVHASTPWG--DLVAQLTGVHYFELGTAITLHLDPAQAYVFGADGRLAQAP 353
           +SGS+T++H  T  G  DLVAQL GVH  ELGT + + +DP + +VFGAD +L  +P
Sbjct: 301 LSGSETYLHLHTLNGGIDLVAQLQGVHQIELGTQLDVFIDPDELFVFGADTKLVSSP 357


Lambda     K      H
   0.318    0.133    0.375 

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: 387
Number of extensions: 19
Number of successful extensions: 4
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: 363
Length of database: 364
Length adjustment: 29
Effective length of query: 334
Effective length of database: 335
Effective search space:   111890
Effective search space used:   111890
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.7 bits)
S2: 49 (23.5 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