Align 2-hydroxymuconate-6-semialdehyde dehydrogenase (EC 1.2.1.85) (characterized)
to candidate WP_043526887.1 JH15_RS03035 aldehyde dehydrogenase
Query= metacyc::MONOMER-15108 (486 letters) >NCBI__GCF_000759345.1:WP_043526887.1 Length = 507 Score = 360 bits (925), Expect = e-104 Identities = 188/476 (39%), Positives = 291/476 (61%), Gaps = 5/476 (1%) Query: 14 FIDGKFVPSLDGKTFDNINPATEEKLGTVAEGGAAEIDLAVQAAKKALN-GPWKKMTANE 72 FID FV +L G TF++INPA + L VA A+ + AV+ A+ A G W ++ Sbjct: 32 FIDDGFVDALSGDTFESINPANGQCLAKVASCDDADAERAVRHARAAFERGEWSRLAPGS 91 Query: 73 RIAVLRKVGDLILERKEELSVLESLDTGKPTWLSGSIDIPRAAYNFHFFSDYIRTITNEA 132 R +L ++ DL+ + K EL+++++LD GKP S D+ + ++ I + E Sbjct: 92 RKRILLRLADLLEQHKHELALIDTLDMGKPIG-SALGDMAGTIACLRYNAESIDKVFGEV 150 Query: 133 TQMDDVALNYAIRRPVGVIGLINPWNLPLLLMTWKLAPALAAGNTVVMKPAELTPMTATV 192 + +L +R P+GV+ I PWN P+++ WK+APALAAGN+V++KP+E +P++A Sbjct: 151 APTGEESLGLVLREPLGVVASIVPWNFPMMMTAWKIAPALAAGNSVILKPSEKSPLSALR 210 Query: 193 LAEICRDAGVPDGVVNLVHGFGPNSAGAALTEHPDVNAISFTGETTTGKIIMASAAKT-L 251 LA++ +DAG+P GV ++ GFG ++ G AL +VN ++FTG T GK +M A ++ L Sbjct: 211 LAQLAQDAGIPRGVFQVLPGFG-HTVGKALALSMEVNCLAFTGSTQVGKQLMQYAGQSNL 269 Query: 252 KRLSYELGGKNPNVIFAD-SNLDEVIETTMKSSFINQGEVCLCGSRIYVERPAYEAFLEK 310 KR+ E GGK+PN++FAD +LD V ++ F NQGEVC+ GSR+ VE E F+ + Sbjct: 270 KRVYLECGGKSPNIVFADCKDLDAVAANAAEAIFHNQGEVCIAGSRLLVENSIREDFVTR 329 Query: 311 FVAKTKELVVGDPFDAKTKVGALISDEHYERVTGYIKLAVEEGGTILTGGKRPEGLEKGY 370 + + + GDP D + +GA++ + ++R+ +I+ VEEG + GG+ E G Sbjct: 330 VLKAAEAMQPGDPLDPDSFMGAIVDETQHKRILDFIRQGVEEGALLRGGGQALETCPGGL 389 Query: 371 FLEPTIITGLTRDCRVVKEEIFGPVVTVIPFDTEEEVLEQINDTHYGLSASVWTNDLRRA 430 F+ PT+ G+T + + +EEIFGPV+ V FDTEEE ++ ND+ YGL+A +W+ D+ R Sbjct: 390 FIAPTVFDGVTPEMSIGREEIFGPVLAVFGFDTEEEAIQLANDSQYGLAAGLWSQDIDRI 449 Query: 431 HRVAGQIEAGIVWVNTWFLRDLRTPFGGMKQSGIGREGGLHSFEFYSELTNICIKL 486 RV ++E+G V+VN W D PFGG+KQSG GR+ +HS YSEL + L Sbjct: 450 MRVTRRLESGQVFVNNWAGGDQTVPFGGVKQSGNGRDKSMHSLAEYSELKTVWFSL 505 Lambda K H 0.318 0.136 0.404 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: 575 Number of extensions: 28 Number of successful extensions: 6 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: 486 Length of database: 507 Length adjustment: 34 Effective length of query: 452 Effective length of database: 473 Effective search space: 213796 Effective search space used: 213796 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: 52 (24.6 bits)
This GapMind analysis is from Sep 24 2021. The underlying query database was built on Sep 17 2021.
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:
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