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: 5 |
NetGPI | no | yes: 0, no: 5 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4QA93
Term | Name | Level | Count |
---|---|---|---|
GO:0000154 | rRNA modification | 6 | 6 |
GO:0001510 | RNA methylation | 4 | 6 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 6 |
GO:0006364 | rRNA processing | 8 | 6 |
GO:0006396 | RNA processing | 6 | 6 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 6 |
GO:0006807 | nitrogen compound metabolic process | 2 | 6 |
GO:0008152 | metabolic process | 1 | 6 |
GO:0009451 | RNA modification | 5 | 6 |
GO:0009987 | cellular process | 1 | 6 |
GO:0016070 | RNA metabolic process | 5 | 6 |
GO:0016072 | rRNA metabolic process | 7 | 6 |
GO:0031167 | rRNA methylation | 5 | 6 |
GO:0032259 | methylation | 2 | 6 |
GO:0034470 | ncRNA processing | 7 | 6 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 6 |
GO:0034660 | ncRNA metabolic process | 6 | 6 |
GO:0043170 | macromolecule metabolic process | 3 | 6 |
GO:0043412 | macromolecule modification | 4 | 6 |
GO:0043414 | macromolecule methylation | 3 | 6 |
GO:0044237 | cellular metabolic process | 2 | 6 |
GO:0044238 | primary metabolic process | 2 | 6 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 6 |
GO:0046483 | heterocycle metabolic process | 3 | 6 |
GO:0070475 | rRNA base methylation | 6 | 6 |
GO:0071704 | organic substance metabolic process | 2 | 6 |
GO:0090304 | nucleic acid metabolic process | 4 | 6 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 6 |
GO:0008168 | methyltransferase activity | 4 | 6 |
GO:0008170 | N-methyltransferase activity | 5 | 6 |
GO:0008173 | RNA methyltransferase activity | 4 | 6 |
GO:0008649 | rRNA methyltransferase activity | 5 | 6 |
GO:0008757 | S-adenosylmethionine-dependent methyltransferase activity | 5 | 6 |
GO:0016436 | rRNA (uridine) methyltransferase activity | 6 | 6 |
GO:0016740 | transferase activity | 2 | 6 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 6 |
GO:0070042 | rRNA (uridine-N3-)-methyltransferase activity | 6 | 6 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 6 |
GO:0140102 | catalytic activity, acting on a rRNA | 4 | 6 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 6 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 504 | 508 | PF00656 | 0.535 |
CLV_NRD_NRD_1 | 100 | 102 | PF00675 | 0.402 |
CLV_NRD_NRD_1 | 214 | 216 | PF00675 | 0.531 |
CLV_NRD_NRD_1 | 377 | 379 | PF00675 | 0.482 |
CLV_NRD_NRD_1 | 432 | 434 | PF00675 | 0.745 |
CLV_NRD_NRD_1 | 491 | 493 | PF00675 | 0.649 |
CLV_NRD_NRD_1 | 51 | 53 | PF00675 | 0.531 |
CLV_NRD_NRD_1 | 556 | 558 | PF00675 | 0.661 |
CLV_NRD_NRD_1 | 64 | 66 | PF00675 | 0.315 |
CLV_NRD_NRD_1 | 83 | 85 | PF00675 | 0.319 |
CLV_PCSK_KEX2_1 | 214 | 216 | PF00082 | 0.531 |
CLV_PCSK_KEX2_1 | 377 | 379 | PF00082 | 0.447 |
CLV_PCSK_KEX2_1 | 42 | 44 | PF00082 | 0.511 |
CLV_PCSK_KEX2_1 | 432 | 434 | PF00082 | 0.745 |
CLV_PCSK_KEX2_1 | 491 | 493 | PF00082 | 0.649 |
CLV_PCSK_KEX2_1 | 51 | 53 | PF00082 | 0.394 |
CLV_PCSK_KEX2_1 | 556 | 558 | PF00082 | 0.661 |
CLV_PCSK_KEX2_1 | 63 | 65 | PF00082 | 0.336 |
CLV_PCSK_KEX2_1 | 99 | 101 | PF00082 | 0.402 |
CLV_PCSK_PC1ET2_1 | 42 | 44 | PF00082 | 0.511 |
CLV_PCSK_PC1ET2_1 | 99 | 101 | PF00082 | 0.402 |
CLV_PCSK_PC7_1 | 373 | 379 | PF00082 | 0.411 |
CLV_PCSK_SKI1_1 | 276 | 280 | PF00082 | 0.563 |
CLV_PCSK_SKI1_1 | 404 | 408 | PF00082 | 0.630 |
CLV_PCSK_SKI1_1 | 416 | 420 | PF00082 | 0.478 |
CLV_PCSK_SKI1_1 | 51 | 55 | PF00082 | 0.494 |
CLV_PCSK_SKI1_1 | 551 | 555 | PF00082 | 0.641 |
CLV_PCSK_SKI1_1 | 556 | 560 | PF00082 | 0.386 |
DEG_SIAH_1 | 14 | 22 | PF03145 | 0.442 |
DOC_MAPK_gen_1 | 377 | 385 | PF00069 | 0.480 |
DOC_MAPK_gen_1 | 63 | 71 | PF00069 | 0.511 |
DOC_MAPK_gen_1 | 84 | 92 | PF00069 | 0.439 |
DOC_MAPK_MEF2A_6 | 63 | 71 | PF00069 | 0.439 |
DOC_PP4_FxxP_1 | 132 | 135 | PF00568 | 0.494 |
DOC_PP4_FxxP_1 | 232 | 235 | PF00568 | 0.518 |
DOC_PP4_FxxP_1 | 345 | 348 | PF00568 | 0.551 |
DOC_USP7_MATH_1 | 190 | 194 | PF00917 | 0.472 |
DOC_USP7_MATH_1 | 2 | 6 | PF00917 | 0.743 |
DOC_USP7_MATH_1 | 202 | 206 | PF00917 | 0.339 |
DOC_USP7_MATH_1 | 283 | 287 | PF00917 | 0.520 |
DOC_USP7_MATH_1 | 80 | 84 | PF00917 | 0.439 |
DOC_USP7_UBL2_3 | 409 | 413 | PF12436 | 0.562 |
DOC_WW_Pin1_4 | 469 | 474 | PF00397 | 0.622 |
DOC_WW_Pin1_4 | 529 | 534 | PF00397 | 0.617 |
DOC_WW_Pin1_4 | 576 | 581 | PF00397 | 0.632 |
LIG_14-3-3_CanoR_1 | 276 | 282 | PF00244 | 0.360 |
LIG_14-3-3_CanoR_1 | 377 | 385 | PF00244 | 0.574 |
LIG_14-3-3_CanoR_1 | 51 | 59 | PF00244 | 0.472 |
LIG_APCC_ABBA_1 | 393 | 398 | PF00400 | 0.635 |
LIG_BRCT_BRCA1_1 | 149 | 153 | PF00533 | 0.494 |
LIG_BRCT_BRCA1_1 | 204 | 208 | PF00533 | 0.494 |
LIG_eIF4E_1 | 143 | 149 | PF01652 | 0.494 |
LIG_FHA_1 | 290 | 296 | PF00498 | 0.709 |
LIG_FHA_1 | 8 | 14 | PF00498 | 0.701 |
LIG_FHA_2 | 249 | 255 | PF00498 | 0.412 |
LIG_FHA_2 | 268 | 274 | PF00498 | 0.417 |
LIG_FHA_2 | 405 | 411 | PF00498 | 0.657 |
LIG_FHA_2 | 454 | 460 | PF00498 | 0.569 |
LIG_FHA_2 | 52 | 58 | PF00498 | 0.522 |
LIG_FHA_2 | 572 | 578 | PF00498 | 0.573 |
LIG_FHA_2 | 72 | 78 | PF00498 | 0.209 |
LIG_LIR_Gen_1 | 124 | 135 | PF02991 | 0.328 |
LIG_LIR_Gen_1 | 193 | 203 | PF02991 | 0.457 |
LIG_LIR_Gen_1 | 22 | 29 | PF02991 | 0.478 |
LIG_LIR_Gen_1 | 268 | 277 | PF02991 | 0.485 |
LIG_LIR_Gen_1 | 35 | 44 | PF02991 | 0.494 |
LIG_LIR_Gen_1 | 362 | 371 | PF02991 | 0.548 |
LIG_LIR_Gen_1 | 477 | 486 | PF02991 | 0.681 |
LIG_LIR_Gen_1 | 507 | 518 | PF02991 | 0.477 |
LIG_LIR_Nem_3 | 124 | 130 | PF02991 | 0.384 |
LIG_LIR_Nem_3 | 140 | 146 | PF02991 | 0.347 |
LIG_LIR_Nem_3 | 193 | 198 | PF02991 | 0.472 |
LIG_LIR_Nem_3 | 205 | 211 | PF02991 | 0.339 |
LIG_LIR_Nem_3 | 22 | 28 | PF02991 | 0.481 |
LIG_LIR_Nem_3 | 268 | 272 | PF02991 | 0.483 |
LIG_LIR_Nem_3 | 273 | 277 | PF02991 | 0.546 |
LIG_LIR_Nem_3 | 280 | 284 | PF02991 | 0.526 |
LIG_LIR_Nem_3 | 35 | 41 | PF02991 | 0.524 |
LIG_LIR_Nem_3 | 353 | 359 | PF02991 | 0.560 |
LIG_LIR_Nem_3 | 362 | 368 | PF02991 | 0.440 |
LIG_LIR_Nem_3 | 477 | 482 | PF02991 | 0.690 |
LIG_LIR_Nem_3 | 507 | 513 | PF02991 | 0.494 |
LIG_MLH1_MIPbox_1 | 149 | 153 | PF16413 | 0.494 |
LIG_MYND_1 | 325 | 329 | PF01753 | 0.539 |
LIG_MYND_1 | 391 | 395 | PF01753 | 0.650 |
LIG_NRBOX | 23 | 29 | PF00104 | 0.322 |
LIG_NRBOX | 401 | 407 | PF00104 | 0.443 |
LIG_PCNA_PIPBox_1 | 145 | 154 | PF02747 | 0.457 |
LIG_PCNA_yPIPBox_3 | 236 | 244 | PF02747 | 0.514 |
LIG_Pex14_1 | 365 | 369 | PF04695 | 0.542 |
LIG_Pex14_2 | 92 | 96 | PF04695 | 0.439 |
LIG_REV1ctd_RIR_1 | 150 | 158 | PF16727 | 0.494 |
LIG_SH2_CRK | 143 | 147 | PF00017 | 0.402 |
LIG_SH2_CRK | 38 | 42 | PF00017 | 0.494 |
LIG_SH2_CRK | 479 | 483 | PF00017 | 0.683 |
LIG_SH2_GRB2like | 211 | 214 | PF00017 | 0.494 |
LIG_SH2_NCK_1 | 269 | 273 | PF00017 | 0.544 |
LIG_SH2_PTP2 | 195 | 198 | PF00017 | 0.439 |
LIG_SH2_SRC | 359 | 362 | PF00017 | 0.484 |
LIG_SH2_SRC | 524 | 527 | PF00017 | 0.596 |
LIG_SH2_STAP1 | 284 | 288 | PF00017 | 0.630 |
LIG_SH2_STAP1 | 524 | 528 | PF00017 | 0.603 |
LIG_SH2_STAT3 | 284 | 287 | PF00017 | 0.646 |
LIG_SH2_STAT3 | 369 | 372 | PF00017 | 0.546 |
LIG_SH2_STAT5 | 195 | 198 | PF00017 | 0.494 |
LIG_SH2_STAT5 | 211 | 214 | PF00017 | 0.258 |
LIG_SH2_STAT5 | 231 | 234 | PF00017 | 0.211 |
LIG_SH2_STAT5 | 269 | 272 | PF00017 | 0.537 |
LIG_SH2_STAT5 | 281 | 284 | PF00017 | 0.415 |
LIG_SH2_STAT5 | 359 | 362 | PF00017 | 0.540 |
LIG_SH2_STAT5 | 417 | 420 | PF00017 | 0.654 |
LIG_SH2_STAT5 | 510 | 513 | PF00017 | 0.472 |
LIG_SH2_STAT5 | 530 | 533 | PF00017 | 0.649 |
LIG_SH2_STAT5 | 95 | 98 | PF00017 | 0.501 |
LIG_SH3_3 | 355 | 361 | PF00018 | 0.500 |
LIG_SH3_3 | 388 | 394 | PF00018 | 0.668 |
LIG_SH3_3 | 470 | 476 | PF00018 | 0.634 |
LIG_SH3_3 | 543 | 549 | PF00018 | 0.635 |
LIG_SUMO_SIM_par_1 | 25 | 31 | PF11976 | 0.494 |
LIG_TRAF2_1 | 523 | 526 | PF00917 | 0.590 |
LIG_TRAF2_1 | 574 | 577 | PF00917 | 0.576 |
LIG_TYR_ITIM | 228 | 233 | PF00017 | 0.507 |
LIG_TYR_ITSM | 475 | 482 | PF00017 | 0.698 |
LIG_UBA3_1 | 401 | 409 | PF00899 | 0.443 |
LIG_WW_2 | 391 | 394 | PF00397 | 0.665 |
MOD_CK1_1 | 114 | 120 | PF00069 | 0.494 |
MOD_CK1_1 | 298 | 304 | PF00069 | 0.696 |
MOD_CK1_1 | 316 | 322 | PF00069 | 0.404 |
MOD_CK1_1 | 346 | 352 | PF00069 | 0.645 |
MOD_CK2_1 | 152 | 158 | PF00069 | 0.439 |
MOD_CK2_1 | 2 | 8 | PF00069 | 0.723 |
MOD_CK2_1 | 248 | 254 | PF00069 | 0.470 |
MOD_CK2_1 | 267 | 273 | PF00069 | 0.395 |
MOD_CK2_1 | 404 | 410 | PF00069 | 0.627 |
MOD_CK2_1 | 441 | 447 | PF00069 | 0.423 |
MOD_CK2_1 | 51 | 57 | PF00069 | 0.375 |
MOD_CK2_1 | 571 | 577 | PF00069 | 0.648 |
MOD_CK2_1 | 75 | 81 | PF00069 | 0.465 |
MOD_GlcNHglycan | 116 | 119 | PF01048 | 0.489 |
MOD_GlcNHglycan | 154 | 157 | PF01048 | 0.527 |
MOD_GlcNHglycan | 192 | 195 | PF01048 | 0.472 |
MOD_GlcNHglycan | 204 | 207 | PF01048 | 0.339 |
MOD_GlcNHglycan | 245 | 249 | PF01048 | 0.469 |
MOD_GlcNHglycan | 294 | 298 | PF01048 | 0.673 |
MOD_GlcNHglycan | 306 | 309 | PF01048 | 0.571 |
MOD_GlcNHglycan | 315 | 318 | PF01048 | 0.516 |
MOD_GlcNHglycan | 46 | 49 | PF01048 | 0.494 |
MOD_GlcNHglycan | 519 | 522 | PF01048 | 0.469 |
MOD_GlcNHglycan | 571 | 574 | PF01048 | 0.687 |
MOD_GSK3_1 | 110 | 117 | PF00069 | 0.494 |
MOD_GSK3_1 | 158 | 165 | PF00069 | 0.413 |
MOD_GSK3_1 | 244 | 251 | PF00069 | 0.397 |
MOD_GSK3_1 | 289 | 296 | PF00069 | 0.598 |
MOD_GSK3_1 | 309 | 316 | PF00069 | 0.494 |
MOD_GSK3_1 | 346 | 353 | PF00069 | 0.642 |
MOD_GSK3_1 | 405 | 412 | PF00069 | 0.606 |
MOD_GSK3_1 | 571 | 578 | PF00069 | 0.603 |
MOD_GSK3_1 | 71 | 78 | PF00069 | 0.503 |
MOD_LATS_1 | 160 | 166 | PF00433 | 0.328 |
MOD_N-GLC_1 | 110 | 115 | PF02516 | 0.494 |
MOD_N-GLC_1 | 313 | 318 | PF02516 | 0.653 |
MOD_N-GLC_1 | 32 | 37 | PF02516 | 0.494 |
MOD_N-GLC_2 | 509 | 511 | PF02516 | 0.371 |
MOD_NEK2_1 | 152 | 157 | PF00069 | 0.494 |
MOD_NEK2_1 | 282 | 287 | PF00069 | 0.576 |
MOD_NEK2_1 | 397 | 402 | PF00069 | 0.557 |
MOD_NEK2_1 | 44 | 49 | PF00069 | 0.377 |
MOD_NEK2_2 | 441 | 446 | PF00069 | 0.424 |
MOD_PIKK_1 | 283 | 289 | PF00454 | 0.608 |
MOD_PIKK_1 | 434 | 440 | PF00454 | 0.544 |
MOD_PIKK_1 | 51 | 57 | PF00454 | 0.439 |
MOD_PKA_1 | 377 | 383 | PF00069 | 0.462 |
MOD_PKA_1 | 42 | 48 | PF00069 | 0.494 |
MOD_PKA_1 | 51 | 57 | PF00069 | 0.362 |
MOD_PKA_2 | 256 | 262 | PF00069 | 0.489 |
MOD_PKA_2 | 377 | 383 | PF00069 | 0.598 |
MOD_PKA_2 | 42 | 48 | PF00069 | 0.494 |
MOD_PKA_2 | 51 | 57 | PF00069 | 0.362 |
MOD_PKA_2 | 562 | 568 | PF00069 | 0.612 |
MOD_Plk_1 | 110 | 116 | PF00069 | 0.494 |
MOD_Plk_1 | 248 | 254 | PF00069 | 0.400 |
MOD_Plk_1 | 309 | 315 | PF00069 | 0.570 |
MOD_Plk_1 | 32 | 38 | PF00069 | 0.494 |
MOD_Plk_1 | 397 | 403 | PF00069 | 0.561 |
MOD_Plk_4 | 248 | 254 | PF00069 | 0.400 |
MOD_Plk_4 | 277 | 283 | PF00069 | 0.370 |
MOD_Plk_4 | 327 | 333 | PF00069 | 0.546 |
MOD_Plk_4 | 361 | 367 | PF00069 | 0.552 |
MOD_Plk_4 | 397 | 403 | PF00069 | 0.596 |
MOD_Plk_4 | 474 | 480 | PF00069 | 0.707 |
MOD_ProDKin_1 | 469 | 475 | PF00069 | 0.624 |
MOD_ProDKin_1 | 529 | 535 | PF00069 | 0.628 |
MOD_ProDKin_1 | 576 | 582 | PF00069 | 0.636 |
TRG_DiLeu_BaEn_2 | 87 | 93 | PF01217 | 0.439 |
TRG_DiLeu_BaLyEn_6 | 322 | 327 | PF01217 | 0.544 |
TRG_DiLeu_BaLyEn_6 | 401 | 406 | PF01217 | 0.448 |
TRG_ENDOCYTIC_2 | 107 | 110 | PF00928 | 0.328 |
TRG_ENDOCYTIC_2 | 143 | 146 | PF00928 | 0.439 |
TRG_ENDOCYTIC_2 | 195 | 198 | PF00928 | 0.494 |
TRG_ENDOCYTIC_2 | 230 | 233 | PF00928 | 0.503 |
TRG_ENDOCYTIC_2 | 269 | 272 | PF00928 | 0.537 |
TRG_ENDOCYTIC_2 | 38 | 41 | PF00928 | 0.531 |
TRG_ENDOCYTIC_2 | 479 | 482 | PF00928 | 0.683 |
TRG_ENDOCYTIC_2 | 510 | 513 | PF00928 | 0.472 |
TRG_ER_diArg_1 | 100 | 103 | PF00400 | 0.489 |
TRG_ER_diArg_1 | 491 | 493 | PF00400 | 0.686 |
TRG_ER_diArg_1 | 50 | 52 | PF00400 | 0.494 |
TRG_ER_diArg_1 | 63 | 65 | PF00400 | 0.302 |
TRG_NLS_Bipartite_1 | 84 | 103 | PF00514 | 0.402 |
TRG_NLS_MonoExtC_3 | 98 | 103 | PF00514 | 0.402 |
TRG_Pf-PMV_PEXEL_1 | 244 | 249 | PF00026 | 0.524 |
TRG_Pf-PMV_PEXEL_1 | 491 | 495 | PF00026 | 0.682 |
TRG_Pf-PMV_PEXEL_1 | 557 | 561 | PF00026 | 0.651 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8ID26 | Leishmania donovani | 88% | 100% |
A4HDV0 | Leishmania braziliensis | 67% | 100% |
A4I145 | Leishmania infantum | 88% | 100% |
E9AXY1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |