GapMind for catabolism of small carbon sources

 

Alignments for a candidate for acn in Pedobacter sp. GW460-11-11-14-LB5

Align Aconitate hydratase (EC 4.2.1.3) (characterized)
to candidate CA265_RS16400 CA265_RS16400 bifunctional aconitate hydratase 2/2-methylisocitrate dehydratase

Query= reanno::Dino:3608667
         (930 letters)



>FitnessBrowser__Pedo557:CA265_RS16400
          Length = 921

 Score = 1420 bits (3676), Expect = 0.0
 Identities = 709/918 (77%), Positives = 807/918 (87%), Gaps = 3/918 (0%)

Query: 1   MSLYTAYLEEIAARKEQGLQPKPIDDAALTSEIIAQIKDPAHEHRADSLQFFIYNTLPGT 60
           MS+Y  Y++EI  RK QGL PKPID A L SEII QIK+  + +R +++ FFIYNTLPGT
Sbjct: 1   MSIYNDYIQEIEDRKAQGLHPKPIDGAELLSEIITQIKNVNNINREEAVNFFIYNTLPGT 60

Query: 61  TSAAGAKAQFLKEIILGESVVAEITPDFAFELLSHMRGGPSVEVLLDIALGDDASLAAQA 120
           T+AA  KAQFLKEIIL E +VAEITPDFAFELLSHM+GGPS++VLLDIAL D+   A +A
Sbjct: 61  TAAAAVKAQFLKEIILAEVIVAEITPDFAFELLSHMKGGPSIKVLLDIALADNGDKAKKA 120

Query: 121 AEVLKTQVFLYEADTDRLKAAHEAGNAVATGILQSYARAEFFTTLPEIEDEIEVVTYIAA 180
           A+VLKTQV+LY+ADTDRLK A+  GN +A  IL+SYA+AEFFT LPE+ +EI+VVT+IA 
Sbjct: 121 ADVLKTQVYLYDADTDRLKDAYNNGNEIAKEILESYAKAEFFTKLPEVAEEIKVVTFIAG 180

Query: 181 EGDISTDLLSPGNQAHSRSDRELHGKCMISEAAQKEIEALKLQHPGKRVMLIAEKGTMGV 240
            GDISTDLLSPGNQAHSRSDRELHGKCMI+  AQ+EI+AL+ QHP K VML+AEKGTMGV
Sbjct: 181 IGDISTDLLSPGNQAHSRSDRELHGKCMITPEAQEEIKALQAQHPDKSVMLVAEKGTMGV 240

Query: 241 GSSRMSGVNNVALWTGKQASPYVPFVNIAPVVAGTNGISPIFMTTVGVTGGIGIDLKNWV 300
           GSSRMSGVNNVALWTGK++SPYVPFVNIAP+V GTNGISPIF+TTV VTGGIGIDL+NWV
Sbjct: 241 GSSRMSGVNNVALWTGKRSSPYVPFVNIAPIVGGTNGISPIFLTTVDVTGGIGIDLQNWV 300

Query: 301 KKVDGDGNPILNNDGNPILEQKYSVDTGTVLKIDTKARKLMSADGGEELADVSSAFSPQA 360
           KK D +GN I N    PILEQ++SV+TGTVL I+TK +KL +  G +EL D+S A +PQ 
Sbjct: 301 KKTDENGNVIRNEKDEPILEQRFSVETGTVLTINTKTKKLYN--GEQELIDISKALTPQK 358

Query: 361 VEFMKAGGSYAVVFGKKLQTLAAETLGVEPTPVFAPAKEISHEGQGLTAVEKIFNANARG 420
           +EFMKAGGSYA++FGKK+QT AA+TLG+E + VFAPAKE+S+EGQGLTAVEKIFN NA G
Sbjct: 359 MEFMKAGGSYAIIFGKKIQTFAAKTLGIEASSVFAPAKEVSYEGQGLTAVEKIFNRNAVG 418

Query: 421 VTPGKVLHAGSDVRVQVNIVGSQDTTGLMTSQELEAMAATVLSPTVDGAYQSGCHTASVW 480
           +T GKVLHAGSDVRV+VNIVGSQDTTGLMT+QELEAMAATV+SP VDGAYQSGCHTASVW
Sbjct: 419 LTQGKVLHAGSDVRVEVNIVGSQDTTGLMTAQELEAMAATVISPIVDGAYQSGCHTASVW 478

Query: 481 DLKAQANTPRLMAFMHKFGLITARDPKGVYHSMTDVIHKVLNDITVSDWDIIIGGDSHTR 540
           D KAQAN P+LM FM+ FG+ITARDPKG YHSMTDVIHKVLNDIT+ +W IIIGGDSHTR
Sbjct: 479 DKKAQANIPKLMKFMNDFGVITARDPKGEYHSMTDVIHKVLNDITIDEWAIIIGGDSHTR 538

Query: 541 MSKGVAFGADSGTVALALATGEATMPIPESVKVTFKGKMADHMDFRDVVHATQAQMLAQH 600
           MSKGVAFGADSGTVALALATGEA+MPIPESVKVTFKG M +HMDFRDVVHATQ QML Q 
Sbjct: 539 MSKGVAFGADSGTVALALATGEASMPIPESVKVTFKGLMKEHMDFRDVVHATQLQMLQQF 598

Query: 601 -GDNVFQGRVIEVHIGTLLADQAFTFTDWTAEMKAKASICISNDDTLIESLEIAKQRIQV 659
            G+NVFQGR+IEVHIGTLLADQAFTFTDWTAEMKAKASICIS DDTLI+SLEIAK RIQ+
Sbjct: 599 DGENVFQGRIIEVHIGTLLADQAFTFTDWTAEMKAKASICISQDDTLIQSLEIAKNRIQI 658

Query: 660 MIDKGMDNDVQMLAGLIAKANARIAEIRSGEKPALKPDDTARYFAEVVVDLDQIVEPMIA 719
           MIDKGMDN  Q+L GLI KAN RI EI++G KPAL PDD A+Y+AEVV+DLD I EPMIA
Sbjct: 659 MIDKGMDNHNQVLQGLINKANKRIEEIKTGIKPALMPDDNAKYYAEVVIDLDLIEEPMIA 718

Query: 720 DPDVHNADVSKRYTHDTIRPISYYGAEKKIDLGFVGSCMVHKGDVKIVAQMLRNLEKANG 779
           DPDV+NADVSKRYTHDTIR +++YG +KK+DLGFVGSCMVHK D+KIV+QML+N+E   G
Sbjct: 719 DPDVNNADVSKRYTHDTIRDLTFYGGDKKVDLGFVGSCMVHKDDLKIVSQMLKNVETQTG 778

Query: 780 EVKFKAPLVLAAPTYNIIDELKEEGDWDVLQKYAGFEFDDSAPKEKARTEYENILYLERP 839
           +V+FKAPLV+AAPTYNIIDELK EGDW+ LQKY+GFEF D+ PK  ARTEYENI+YLERP
Sbjct: 779 KVEFKAPLVVAAPTYNIIDELKAEGDWEYLQKYSGFEFSDALPKSAARTEYENIMYLERP 838

Query: 840 GCNLCMGNQEKAAKGDTVLATSTRLFQGRVVADSETKKGESLLGSTPVVVLSAILGRTPT 899
           GCNLCMGNQEKAAKGDTV+ATSTRLFQGRVV D + KKGESLL STPVVVLSAILGR P+
Sbjct: 839 GCNLCMGNQEKAAKGDTVMATSTRLFQGRVVEDKDGKKGESLLASTPVVVLSAILGRIPS 898

Query: 900 VEEYKTAVEGINLTKFAP 917
           +EEYK AVEGINLTKF P
Sbjct: 899 IEEYKVAVEGINLTKFTP 916


Lambda     K      H
   0.316    0.132    0.374 

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: 2223
Number of extensions: 83
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: 930
Length of database: 921
Length adjustment: 43
Effective length of query: 887
Effective length of database: 878
Effective search space:   778786
Effective search space used:   778786
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 (21.6 bits)
S2: 57 (26.6 bits)

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

Links

Downloads

Related tools

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