Polymerase, mitochondrial DNA primase PRI1
Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005654 | nucleoplasm | 2 | 1 |
GO:0005730 | nucleolus | 5 | 1 |
GO:0005759 | mitochondrial matrix | 5 | 1 |
GO:0020023 | kinetoplast | 2 | 1 |
GO:0031974 | membrane-enclosed lumen | 2 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:0043233 | organelle lumen | 3 | 1 |
GO:0070013 | intracellular organelle lumen | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4I0B9
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006259 | DNA metabolic process | 4 | 1 |
GO:0006260 | DNA replication | 5 | 1 |
GO:0006261 | DNA-templated DNA replication | 6 | 1 |
GO:0006264 | mitochondrial DNA replication | 6 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0032042 | mitochondrial DNA metabolic process | 5 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 7 |
GO:0003899 | DNA-directed 5'-3' RNA polymerase activity | 6 | 5 |
GO:0016740 | transferase activity | 2 | 5 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 5 |
GO:0016779 | nucleotidyltransferase activity | 4 | 5 |
GO:0016787 | hydrolase activity | 2 | 7 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 7 |
GO:0034062 | 5'-3' RNA polymerase activity | 5 | 5 |
GO:0097747 | RNA polymerase activity | 4 | 5 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 5 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 5 |
GO:0003896 | DNA primase activity | 7 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 271 | 275 | PF00656 | 0.474 |
CLV_C14_Caspase3-7 | 572 | 576 | PF00656 | 0.310 |
CLV_NRD_NRD_1 | 101 | 103 | PF00675 | 0.537 |
CLV_NRD_NRD_1 | 147 | 149 | PF00675 | 0.604 |
CLV_NRD_NRD_1 | 156 | 158 | PF00675 | 0.572 |
CLV_NRD_NRD_1 | 252 | 254 | PF00675 | 0.658 |
CLV_NRD_NRD_1 | 279 | 281 | PF00675 | 0.405 |
CLV_NRD_NRD_1 | 348 | 350 | PF00675 | 0.379 |
CLV_NRD_NRD_1 | 581 | 583 | PF00675 | 0.310 |
CLV_NRD_NRD_1 | 671 | 673 | PF00675 | 0.577 |
CLV_NRD_NRD_1 | 682 | 684 | PF00675 | 0.587 |
CLV_NRD_NRD_1 | 90 | 92 | PF00675 | 0.531 |
CLV_NRD_NRD_1 | 97 | 99 | PF00675 | 0.527 |
CLV_PCSK_KEX2_1 | 101 | 103 | PF00082 | 0.518 |
CLV_PCSK_KEX2_1 | 147 | 149 | PF00082 | 0.529 |
CLV_PCSK_KEX2_1 | 19 | 21 | PF00082 | 0.660 |
CLV_PCSK_KEX2_1 | 279 | 281 | PF00082 | 0.405 |
CLV_PCSK_KEX2_1 | 616 | 618 | PF00082 | 0.471 |
CLV_PCSK_KEX2_1 | 682 | 684 | PF00082 | 0.606 |
CLV_PCSK_KEX2_1 | 97 | 99 | PF00082 | 0.514 |
CLV_PCSK_PC1ET2_1 | 101 | 103 | PF00082 | 0.518 |
CLV_PCSK_PC1ET2_1 | 19 | 21 | PF00082 | 0.571 |
CLV_PCSK_PC1ET2_1 | 616 | 618 | PF00082 | 0.471 |
CLV_PCSK_PC7_1 | 97 | 103 | PF00082 | 0.514 |
CLV_PCSK_SKI1_1 | 349 | 353 | PF00082 | 0.368 |
CLV_PCSK_SKI1_1 | 479 | 483 | PF00082 | 0.433 |
CLV_PCSK_SKI1_1 | 532 | 536 | PF00082 | 0.383 |
CLV_PCSK_SKI1_1 | 672 | 676 | PF00082 | 0.579 |
CLV_PCSK_SKI1_1 | 678 | 682 | PF00082 | 0.585 |
CLV_PCSK_SKI1_1 | 8 | 12 | PF00082 | 0.550 |
CLV_PCSK_SKI1_1 | 98 | 102 | PF00082 | 0.510 |
DEG_APCC_DBOX_1 | 146 | 154 | PF00400 | 0.527 |
DEG_APCC_DBOX_1 | 348 | 356 | PF00400 | 0.362 |
DEG_APCC_KENBOX_2 | 434 | 438 | PF00400 | 0.421 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.527 |
DEG_SCF_FBW7_2 | 355 | 361 | PF00400 | 0.419 |
DEG_SIAH_1 | 72 | 80 | PF03145 | 0.520 |
DOC_ANK_TNKS_1 | 156 | 163 | PF00023 | 0.603 |
DOC_CKS1_1 | 292 | 297 | PF01111 | 0.394 |
DOC_CKS1_1 | 355 | 360 | PF01111 | 0.415 |
DOC_CYCLIN_RxL_1 | 476 | 484 | PF00134 | 0.405 |
DOC_CYCLIN_yCln2_LP_2 | 565 | 571 | PF00134 | 0.358 |
DOC_MAPK_DCC_7 | 409 | 419 | PF00069 | 0.382 |
DOC_MAPK_gen_1 | 435 | 445 | PF00069 | 0.467 |
DOC_MAPK_gen_1 | 529 | 539 | PF00069 | 0.310 |
DOC_MAPK_gen_1 | 582 | 588 | PF00069 | 0.383 |
DOC_MAPK_gen_1 | 616 | 623 | PF00069 | 0.485 |
DOC_MAPK_HePTP_8 | 316 | 328 | PF00069 | 0.359 |
DOC_MAPK_MEF2A_6 | 319 | 328 | PF00069 | 0.361 |
DOC_MAPK_MEF2A_6 | 413 | 421 | PF00069 | 0.455 |
DOC_MAPK_MEF2A_6 | 543 | 550 | PF00069 | 0.310 |
DOC_MAPK_MEF2A_6 | 616 | 625 | PF00069 | 0.497 |
DOC_MAPK_NFAT4_5 | 543 | 551 | PF00069 | 0.310 |
DOC_PP1_RVXF_1 | 477 | 484 | PF00149 | 0.408 |
DOC_PP2B_LxvP_1 | 509 | 512 | PF13499 | 0.591 |
DOC_PP2B_LxvP_1 | 621 | 624 | PF13499 | 0.512 |
DOC_PP2B_LxvP_1 | 69 | 72 | PF13499 | 0.558 |
DOC_PP4_FxxP_1 | 289 | 292 | PF00568 | 0.370 |
DOC_PP4_FxxP_1 | 445 | 448 | PF00568 | 0.361 |
DOC_PP4_FxxP_1 | 483 | 486 | PF00568 | 0.434 |
DOC_PP4_MxPP_1 | 47 | 50 | PF00568 | 0.557 |
DOC_USP7_MATH_1 | 130 | 134 | PF00917 | 0.563 |
DOC_USP7_MATH_1 | 160 | 164 | PF00917 | 0.618 |
DOC_USP7_MATH_1 | 217 | 221 | PF00917 | 0.572 |
DOC_USP7_MATH_1 | 234 | 238 | PF00917 | 0.571 |
DOC_USP7_MATH_1 | 268 | 272 | PF00917 | 0.495 |
DOC_USP7_MATH_1 | 297 | 301 | PF00917 | 0.436 |
DOC_USP7_MATH_1 | 30 | 34 | PF00917 | 0.557 |
DOC_USP7_MATH_1 | 302 | 306 | PF00917 | 0.455 |
DOC_USP7_MATH_1 | 465 | 469 | PF00917 | 0.386 |
DOC_USP7_MATH_1 | 59 | 63 | PF00917 | 0.619 |
DOC_USP7_MATH_1 | 663 | 667 | PF00917 | 0.602 |
DOC_USP7_MATH_1 | 73 | 77 | PF00917 | 0.500 |
DOC_USP7_UBL2_3 | 583 | 587 | PF12436 | 0.310 |
DOC_USP7_UBL2_3 | 675 | 679 | PF12436 | 0.577 |
DOC_WW_Pin1_4 | 178 | 183 | PF00397 | 0.594 |
DOC_WW_Pin1_4 | 291 | 296 | PF00397 | 0.412 |
DOC_WW_Pin1_4 | 319 | 324 | PF00397 | 0.412 |
DOC_WW_Pin1_4 | 354 | 359 | PF00397 | 0.412 |
DOC_WW_Pin1_4 | 375 | 380 | PF00397 | 0.370 |
DOC_WW_Pin1_4 | 45 | 50 | PF00397 | 0.593 |
LIG_14-3-3_CanoR_1 | 102 | 112 | PF00244 | 0.513 |
LIG_14-3-3_CanoR_1 | 253 | 261 | PF00244 | 0.501 |
LIG_14-3-3_CanoR_1 | 3 | 10 | PF00244 | 0.535 |
LIG_14-3-3_CanoR_1 | 438 | 445 | PF00244 | 0.454 |
LIG_14-3-3_CanoR_1 | 479 | 484 | PF00244 | 0.414 |
LIG_14-3-3_CanoR_1 | 532 | 539 | PF00244 | 0.460 |
LIG_14-3-3_CanoR_1 | 65 | 70 | PF00244 | 0.547 |
LIG_Actin_WH2_2 | 367 | 384 | PF00022 | 0.383 |
LIG_APCC_ABBA_1 | 442 | 447 | PF00400 | 0.371 |
LIG_deltaCOP1_diTrp_1 | 446 | 454 | PF00928 | 0.389 |
LIG_deltaCOP1_diTrp_1 | 541 | 545 | PF00928 | 0.351 |
LIG_deltaCOP1_diTrp_1 | 594 | 600 | PF00928 | 0.310 |
LIG_FHA_1 | 253 | 259 | PF00498 | 0.478 |
LIG_FHA_1 | 370 | 376 | PF00498 | 0.368 |
LIG_FHA_1 | 437 | 443 | PF00498 | 0.396 |
LIG_FHA_2 | 320 | 326 | PF00498 | 0.438 |
LIG_FHA_2 | 517 | 523 | PF00498 | 0.422 |
LIG_FHA_2 | 533 | 539 | PF00498 | 0.383 |
LIG_LIR_Apic_2 | 482 | 486 | PF02991 | 0.439 |
LIG_LIR_Gen_1 | 238 | 245 | PF02991 | 0.560 |
LIG_LIR_Gen_1 | 394 | 403 | PF02991 | 0.357 |
LIG_LIR_Gen_1 | 475 | 485 | PF02991 | 0.479 |
LIG_LIR_Gen_1 | 594 | 605 | PF02991 | 0.310 |
LIG_LIR_Nem_3 | 238 | 244 | PF02991 | 0.557 |
LIG_LIR_Nem_3 | 394 | 400 | PF02991 | 0.373 |
LIG_LIR_Nem_3 | 475 | 480 | PF02991 | 0.475 |
LIG_LIR_Nem_3 | 544 | 548 | PF02991 | 0.310 |
LIG_LIR_Nem_3 | 594 | 600 | PF02991 | 0.310 |
LIG_LIR_Nem_3 | 609 | 615 | PF02991 | 0.310 |
LIG_LRP6_Inhibitor_1 | 151 | 157 | PF00058 | 0.510 |
LIG_MAD2 | 350 | 358 | PF02301 | 0.438 |
LIG_OCRL_FandH_1 | 399 | 411 | PF00620 | 0.334 |
LIG_Pex14_1 | 450 | 454 | PF04695 | 0.375 |
LIG_Pex14_1 | 611 | 615 | PF04695 | 0.310 |
LIG_Pex14_2 | 10 | 14 | PF04695 | 0.557 |
LIG_Pex14_2 | 406 | 410 | PF04695 | 0.354 |
LIG_SH2_CRK | 241 | 245 | PF00017 | 0.542 |
LIG_SH2_CRK | 615 | 619 | PF00017 | 0.456 |
LIG_SH2_NCK_1 | 241 | 245 | PF00017 | 0.542 |
LIG_SH2_STAP1 | 241 | 245 | PF00017 | 0.559 |
LIG_SH2_STAP1 | 608 | 612 | PF00017 | 0.258 |
LIG_SH3_3 | 120 | 126 | PF00018 | 0.647 |
LIG_SH3_3 | 129 | 135 | PF00018 | 0.553 |
LIG_SH3_3 | 289 | 295 | PF00018 | 0.385 |
LIG_SH3_3 | 301 | 307 | PF00018 | 0.482 |
LIG_SH3_3 | 352 | 358 | PF00018 | 0.437 |
LIG_SH3_3 | 468 | 474 | PF00018 | 0.436 |
LIG_SH3_3 | 511 | 517 | PF00018 | 0.532 |
LIG_SH3_3 | 649 | 655 | PF00018 | 0.584 |
LIG_SH3_3 | 67 | 73 | PF00018 | 0.564 |
LIG_SUMO_SIM_anti_2 | 322 | 329 | PF11976 | 0.348 |
LIG_TRAF2_1 | 163 | 166 | PF00917 | 0.766 |
LIG_UBA3_1 | 152 | 158 | PF00899 | 0.578 |
LIG_UBA3_1 | 427 | 435 | PF00899 | 0.370 |
LIG_UBA3_1 | 95 | 104 | PF00899 | 0.515 |
LIG_WRC_WIRS_1 | 480 | 485 | PF05994 | 0.486 |
LIG_WW_3 | 144 | 148 | PF00397 | 0.548 |
MOD_CDK_SPxK_1 | 178 | 184 | PF00069 | 0.587 |
MOD_CDK_SPxK_1 | 354 | 360 | PF00069 | 0.419 |
MOD_CDK_SPxxK_3 | 375 | 382 | PF00069 | 0.381 |
MOD_CK1_1 | 176 | 182 | PF00069 | 0.671 |
MOD_CK1_1 | 197 | 203 | PF00069 | 0.752 |
MOD_CK1_1 | 252 | 258 | PF00069 | 0.516 |
MOD_CK1_1 | 45 | 51 | PF00069 | 0.564 |
MOD_CK1_1 | 475 | 481 | PF00069 | 0.475 |
MOD_CK1_1 | 666 | 672 | PF00069 | 0.653 |
MOD_CK2_1 | 160 | 166 | PF00069 | 0.624 |
MOD_CK2_1 | 222 | 228 | PF00069 | 0.732 |
MOD_CK2_1 | 516 | 522 | PF00069 | 0.453 |
MOD_CK2_1 | 532 | 538 | PF00069 | 0.310 |
MOD_CMANNOS | 542 | 545 | PF00535 | 0.310 |
MOD_DYRK1A_RPxSP_1 | 319 | 323 | PF00069 | 0.450 |
MOD_GlcNHglycan | 105 | 108 | PF01048 | 0.562 |
MOD_GlcNHglycan | 225 | 228 | PF01048 | 0.777 |
MOD_GlcNHglycan | 24 | 27 | PF01048 | 0.497 |
MOD_GlcNHglycan | 282 | 285 | PF01048 | 0.459 |
MOD_GlcNHglycan | 300 | 303 | PF01048 | 0.463 |
MOD_GlcNHglycan | 439 | 442 | PF01048 | 0.379 |
MOD_GlcNHglycan | 5 | 8 | PF01048 | 0.531 |
MOD_GlcNHglycan | 589 | 592 | PF01048 | 0.345 |
MOD_GlcNHglycan | 612 | 615 | PF01048 | 0.345 |
MOD_GlcNHglycan | 65 | 68 | PF01048 | 0.587 |
MOD_GlcNHglycan | 668 | 671 | PF01048 | 0.614 |
MOD_GlcNHglycan | 73 | 76 | PF01048 | 0.522 |
MOD_GlcNHglycan | 79 | 82 | PF01048 | 0.521 |
MOD_GSK3_1 | 169 | 176 | PF00069 | 0.684 |
MOD_GSK3_1 | 18 | 25 | PF00069 | 0.515 |
MOD_GSK3_1 | 211 | 218 | PF00069 | 0.702 |
MOD_GSK3_1 | 248 | 255 | PF00069 | 0.629 |
MOD_GSK3_1 | 298 | 305 | PF00069 | 0.425 |
MOD_GSK3_1 | 475 | 482 | PF00069 | 0.444 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.566 |
MOD_GSK3_1 | 606 | 613 | PF00069 | 0.345 |
MOD_GSK3_1 | 73 | 80 | PF00069 | 0.505 |
MOD_N-GLC_1 | 22 | 27 | PF02516 | 0.560 |
MOD_N-GLC_1 | 246 | 251 | PF02516 | 0.655 |
MOD_N-GLC_1 | 436 | 441 | PF02516 | 0.415 |
MOD_N-GLC_1 | 525 | 530 | PF02516 | 0.261 |
MOD_NEK2_1 | 63 | 68 | PF00069 | 0.602 |
MOD_PIKK_1 | 121 | 127 | PF00454 | 0.783 |
MOD_PIKK_1 | 194 | 200 | PF00454 | 0.641 |
MOD_PIKK_1 | 369 | 375 | PF00454 | 0.379 |
MOD_PKA_1 | 103 | 109 | PF00069 | 0.551 |
MOD_PKA_1 | 19 | 25 | PF00069 | 0.553 |
MOD_PKA_1 | 382 | 388 | PF00069 | 0.363 |
MOD_PKA_2 | 19 | 25 | PF00069 | 0.540 |
MOD_PKA_2 | 2 | 8 | PF00069 | 0.519 |
MOD_PKA_2 | 252 | 258 | PF00069 | 0.531 |
MOD_PKA_2 | 437 | 443 | PF00069 | 0.469 |
MOD_Plk_1 | 525 | 531 | PF00069 | 0.261 |
MOD_Plk_2-3 | 173 | 179 | PF00069 | 0.710 |
MOD_Plk_4 | 65 | 71 | PF00069 | 0.544 |
MOD_ProDKin_1 | 178 | 184 | PF00069 | 0.594 |
MOD_ProDKin_1 | 291 | 297 | PF00069 | 0.415 |
MOD_ProDKin_1 | 319 | 325 | PF00069 | 0.410 |
MOD_ProDKin_1 | 354 | 360 | PF00069 | 0.419 |
MOD_ProDKin_1 | 375 | 381 | PF00069 | 0.376 |
MOD_ProDKin_1 | 45 | 51 | PF00069 | 0.594 |
MOD_SUMO_for_1 | 359 | 362 | PF00179 | 0.382 |
MOD_SUMO_rev_2 | 161 | 168 | PF00179 | 0.603 |
TRG_ENDOCYTIC_2 | 241 | 244 | PF00928 | 0.569 |
TRG_ENDOCYTIC_2 | 338 | 341 | PF00928 | 0.408 |
TRG_ENDOCYTIC_2 | 615 | 618 | PF00928 | 0.386 |
TRG_ER_diArg_1 | 146 | 148 | PF00400 | 0.539 |
TRG_ER_diArg_1 | 279 | 281 | PF00400 | 0.405 |
TRG_ER_diArg_1 | 681 | 683 | PF00400 | 0.657 |
TRG_ER_diArg_1 | 96 | 98 | PF00400 | 0.517 |
TRG_NES_CRM1_1 | 364 | 377 | PF08389 | 0.387 |
TRG_NLS_Bipartite_1 | 91 | 106 | PF00514 | 0.520 |
TRG_NLS_MonoCore_2 | 100 | 105 | PF00514 | 0.541 |
TRG_NLS_MonoCore_2 | 90 | 95 | PF00514 | 0.519 |
TRG_NLS_MonoExtN_4 | 88 | 95 | PF00514 | 0.539 |
TRG_NLS_MonoExtN_4 | 98 | 105 | PF00514 | 0.505 |
TRG_Pf-PMV_PEXEL_1 | 479 | 484 | PF00026 | 0.487 |
TRG_Pf-PMV_PEXEL_1 | 529 | 533 | PF00026 | 0.414 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I0R5 | Leptomonas seymouri | 60% | 98% |
A0A3S7WXR7 | Leishmania donovani | 100% | 100% |
A4HCT9 | Leishmania braziliensis | 82% | 100% |
E9AW83 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
Q4QB95 | Leishmania major | 93% | 100% |