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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4QJA1
Term | Name | Level | Count |
---|---|---|---|
GO:0001510 | RNA methylation | 4 | 9 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 9 |
GO:0006396 | RNA processing | 6 | 9 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 9 |
GO:0006807 | nitrogen compound metabolic process | 2 | 9 |
GO:0008152 | metabolic process | 1 | 9 |
GO:0009451 | RNA modification | 5 | 9 |
GO:0009987 | cellular process | 1 | 9 |
GO:0016070 | RNA metabolic process | 5 | 9 |
GO:0032259 | methylation | 2 | 9 |
GO:0034470 | ncRNA processing | 7 | 9 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 9 |
GO:0034660 | ncRNA metabolic process | 6 | 9 |
GO:0043170 | macromolecule metabolic process | 3 | 9 |
GO:0043412 | macromolecule modification | 4 | 9 |
GO:0043414 | macromolecule methylation | 3 | 9 |
GO:0044237 | cellular metabolic process | 2 | 9 |
GO:0044238 | primary metabolic process | 2 | 9 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 9 |
GO:0046483 | heterocycle metabolic process | 3 | 9 |
GO:0071704 | organic substance metabolic process | 2 | 9 |
GO:0090304 | nucleic acid metabolic process | 4 | 9 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 11 |
GO:0003824 | catalytic activity | 1 | 11 |
GO:0004809 | tRNA (guanine-N2-)-methyltransferase activity | 6 | 2 |
GO:0005488 | binding | 1 | 11 |
GO:0008168 | methyltransferase activity | 4 | 11 |
GO:0008170 | N-methyltransferase activity | 5 | 2 |
GO:0008173 | RNA methyltransferase activity | 4 | 2 |
GO:0008175 | tRNA methyltransferase activity | 5 | 2 |
GO:0008757 | S-adenosylmethionine-dependent methyltransferase activity | 5 | 2 |
GO:0016423 | tRNA (guanine) methyltransferase activity | 6 | 2 |
GO:0016740 | transferase activity | 2 | 11 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 11 |
GO:0097159 | organic cyclic compound binding | 2 | 11 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 2 |
GO:0140101 | catalytic activity, acting on a tRNA | 4 | 2 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 2 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 277 | 281 | PF00656 | 0.503 |
CLV_C14_Caspase3-7 | 516 | 520 | PF00656 | 0.580 |
CLV_C14_Caspase3-7 | 561 | 565 | PF00656 | 0.783 |
CLV_C14_Caspase3-7 | 574 | 578 | PF00656 | 0.587 |
CLV_MEL_PAP_1 | 468 | 474 | PF00089 | 0.484 |
CLV_NRD_NRD_1 | 222 | 224 | PF00675 | 0.457 |
CLV_NRD_NRD_1 | 301 | 303 | PF00675 | 0.337 |
CLV_NRD_NRD_1 | 379 | 381 | PF00675 | 0.259 |
CLV_NRD_NRD_1 | 478 | 480 | PF00675 | 0.378 |
CLV_NRD_NRD_1 | 483 | 485 | PF00675 | 0.407 |
CLV_NRD_NRD_1 | 531 | 533 | PF00675 | 0.586 |
CLV_NRD_NRD_1 | 568 | 570 | PF00675 | 0.691 |
CLV_PCSK_FUR_1 | 527 | 531 | PF00082 | 0.627 |
CLV_PCSK_KEX2_1 | 149 | 151 | PF00082 | 0.469 |
CLV_PCSK_KEX2_1 | 158 | 160 | PF00082 | 0.365 |
CLV_PCSK_KEX2_1 | 224 | 226 | PF00082 | 0.255 |
CLV_PCSK_KEX2_1 | 301 | 303 | PF00082 | 0.321 |
CLV_PCSK_KEX2_1 | 381 | 383 | PF00082 | 0.289 |
CLV_PCSK_KEX2_1 | 478 | 480 | PF00082 | 0.382 |
CLV_PCSK_KEX2_1 | 529 | 531 | PF00082 | 0.549 |
CLV_PCSK_KEX2_1 | 533 | 535 | PF00082 | 0.525 |
CLV_PCSK_KEX2_1 | 568 | 570 | PF00082 | 0.723 |
CLV_PCSK_PC1ET2_1 | 149 | 151 | PF00082 | 0.518 |
CLV_PCSK_PC1ET2_1 | 158 | 160 | PF00082 | 0.504 |
CLV_PCSK_PC1ET2_1 | 224 | 226 | PF00082 | 0.273 |
CLV_PCSK_PC1ET2_1 | 381 | 383 | PF00082 | 0.323 |
CLV_PCSK_PC1ET2_1 | 529 | 531 | PF00082 | 0.549 |
CLV_PCSK_PC1ET2_1 | 533 | 535 | PF00082 | 0.525 |
CLV_PCSK_PC7_1 | 377 | 383 | PF00082 | 0.278 |
CLV_PCSK_SKI1_1 | 213 | 217 | PF00082 | 0.493 |
CLV_PCSK_SKI1_1 | 302 | 306 | PF00082 | 0.337 |
CLV_PCSK_SKI1_1 | 593 | 597 | PF00082 | 0.638 |
CLV_PCSK_SKI1_1 | 69 | 73 | PF00082 | 0.326 |
DEG_APCC_DBOX_1 | 470 | 478 | PF00400 | 0.422 |
DEG_APCC_DBOX_1 | 59 | 67 | PF00400 | 0.522 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.445 |
DOC_CDC14_PxL_1 | 80 | 88 | PF14671 | 0.447 |
DOC_CKS1_1 | 550 | 555 | PF01111 | 0.731 |
DOC_CYCLIN_RxL_1 | 298 | 309 | PF00134 | 0.521 |
DOC_CYCLIN_yCln2_LP_2 | 28 | 34 | PF00134 | 0.483 |
DOC_MAPK_gen_1 | 475 | 483 | PF00069 | 0.480 |
DOC_MAPK_gen_1 | 502 | 510 | PF00069 | 0.506 |
DOC_MAPK_MEF2A_6 | 503 | 512 | PF00069 | 0.621 |
DOC_MAPK_RevD_3 | 472 | 485 | PF00069 | 0.461 |
DOC_PP2B_LxvP_1 | 28 | 31 | PF13499 | 0.483 |
DOC_PP2B_LxvP_1 | 335 | 338 | PF13499 | 0.471 |
DOC_PP4_FxxP_1 | 16 | 19 | PF00568 | 0.412 |
DOC_PP4_FxxP_1 | 443 | 446 | PF00568 | 0.403 |
DOC_PP4_FxxP_1 | 54 | 57 | PF00568 | 0.480 |
DOC_USP7_MATH_1 | 104 | 108 | PF00917 | 0.596 |
DOC_USP7_MATH_1 | 235 | 239 | PF00917 | 0.537 |
DOC_USP7_MATH_1 | 396 | 400 | PF00917 | 0.690 |
DOC_USP7_MATH_1 | 544 | 548 | PF00917 | 0.712 |
DOC_USP7_MATH_1 | 58 | 62 | PF00917 | 0.533 |
DOC_USP7_UBL2_3 | 529 | 533 | PF12436 | 0.539 |
DOC_WW_Pin1_4 | 108 | 113 | PF00397 | 0.692 |
DOC_WW_Pin1_4 | 291 | 296 | PF00397 | 0.537 |
DOC_WW_Pin1_4 | 501 | 506 | PF00397 | 0.632 |
DOC_WW_Pin1_4 | 53 | 58 | PF00397 | 0.502 |
DOC_WW_Pin1_4 | 546 | 551 | PF00397 | 0.637 |
LIG_14-3-3_CanoR_1 | 342 | 352 | PF00244 | 0.510 |
LIG_14-3-3_CanoR_1 | 471 | 475 | PF00244 | 0.426 |
LIG_14-3-3_CanoR_1 | 74 | 80 | PF00244 | 0.479 |
LIG_Actin_WH2_2 | 461 | 477 | PF00022 | 0.398 |
LIG_Actin_WH2_2 | 59 | 76 | PF00022 | 0.401 |
LIG_AP2alpha_2 | 255 | 257 | PF02296 | 0.458 |
LIG_BIR_III_4 | 278 | 282 | PF00653 | 0.488 |
LIG_CSL_BTD_1 | 443 | 446 | PF09270 | 0.472 |
LIG_deltaCOP1_diTrp_1 | 47 | 54 | PF00928 | 0.493 |
LIG_FHA_1 | 115 | 121 | PF00498 | 0.527 |
LIG_FHA_1 | 123 | 129 | PF00498 | 0.441 |
LIG_FHA_1 | 217 | 223 | PF00498 | 0.417 |
LIG_FHA_1 | 25 | 31 | PF00498 | 0.409 |
LIG_FHA_1 | 258 | 264 | PF00498 | 0.458 |
LIG_FHA_1 | 418 | 424 | PF00498 | 0.435 |
LIG_FHA_1 | 431 | 437 | PF00498 | 0.457 |
LIG_FHA_2 | 31 | 37 | PF00498 | 0.473 |
LIG_FHA_2 | 315 | 321 | PF00498 | 0.488 |
LIG_FHA_2 | 450 | 456 | PF00498 | 0.457 |
LIG_FHA_2 | 76 | 82 | PF00498 | 0.456 |
LIG_FHA_2 | 83 | 89 | PF00498 | 0.446 |
LIG_LIR_Apic_2 | 15 | 19 | PF02991 | 0.443 |
LIG_LIR_Apic_2 | 165 | 171 | PF02991 | 0.551 |
LIG_LIR_Apic_2 | 442 | 446 | PF02991 | 0.428 |
LIG_LIR_Apic_2 | 52 | 57 | PF02991 | 0.503 |
LIG_LIR_Gen_1 | 20 | 28 | PF02991 | 0.463 |
LIG_LIR_Gen_1 | 433 | 441 | PF02991 | 0.420 |
LIG_LIR_Gen_1 | 48 | 58 | PF02991 | 0.393 |
LIG_LIR_Gen_1 | 87 | 95 | PF02991 | 0.502 |
LIG_LIR_LC3C_4 | 433 | 437 | PF02991 | 0.426 |
LIG_LIR_Nem_3 | 20 | 24 | PF02991 | 0.450 |
LIG_LIR_Nem_3 | 328 | 333 | PF02991 | 0.470 |
LIG_LIR_Nem_3 | 414 | 418 | PF02991 | 0.563 |
LIG_LIR_Nem_3 | 433 | 437 | PF02991 | 0.471 |
LIG_LIR_Nem_3 | 47 | 53 | PF02991 | 0.430 |
LIG_LIR_Nem_3 | 522 | 526 | PF02991 | 0.565 |
LIG_LIR_Nem_3 | 87 | 93 | PF02991 | 0.490 |
LIG_PCNA_yPIPBox_3 | 196 | 206 | PF02747 | 0.486 |
LIG_Pex14_1 | 50 | 54 | PF04695 | 0.458 |
LIG_SH2_CRK | 333 | 337 | PF00017 | 0.537 |
LIG_SH2_GRB2like | 451 | 454 | PF00017 | 0.360 |
LIG_SH2_PTP2 | 176 | 179 | PF00017 | 0.501 |
LIG_SH2_PTP2 | 3 | 6 | PF00017 | 0.465 |
LIG_SH2_PTP2 | 90 | 93 | PF00017 | 0.488 |
LIG_SH2_STAP1 | 133 | 137 | PF00017 | 0.495 |
LIG_SH2_STAP1 | 144 | 148 | PF00017 | 0.556 |
LIG_SH2_STAT3 | 133 | 136 | PF00017 | 0.494 |
LIG_SH2_STAT5 | 176 | 179 | PF00017 | 0.470 |
LIG_SH2_STAT5 | 227 | 230 | PF00017 | 0.458 |
LIG_SH2_STAT5 | 252 | 255 | PF00017 | 0.488 |
LIG_SH2_STAT5 | 3 | 6 | PF00017 | 0.409 |
LIG_SH2_STAT5 | 308 | 311 | PF00017 | 0.521 |
LIG_SH2_STAT5 | 434 | 437 | PF00017 | 0.461 |
LIG_SH2_STAT5 | 451 | 454 | PF00017 | 0.374 |
LIG_SH2_STAT5 | 77 | 80 | PF00017 | 0.371 |
LIG_SH2_STAT5 | 90 | 93 | PF00017 | 0.428 |
LIG_SH3_3 | 180 | 186 | PF00018 | 0.526 |
LIG_SH3_3 | 250 | 256 | PF00018 | 0.476 |
LIG_SH3_3 | 454 | 460 | PF00018 | 0.409 |
LIG_SH3_3 | 486 | 492 | PF00018 | 0.532 |
LIG_SH3_3 | 547 | 553 | PF00018 | 0.668 |
LIG_SUMO_SIM_anti_2 | 461 | 467 | PF11976 | 0.423 |
LIG_TRAF2_1 | 234 | 237 | PF00917 | 0.537 |
LIG_TRAF2_1 | 317 | 320 | PF00917 | 0.510 |
LIG_TRFH_1 | 333 | 337 | PF08558 | 0.488 |
LIG_UBA3_1 | 480 | 485 | PF00899 | 0.411 |
MOD_CDK_SPxxK_3 | 53 | 60 | PF00069 | 0.513 |
MOD_CK1_1 | 107 | 113 | PF00069 | 0.641 |
MOD_CK1_1 | 131 | 137 | PF00069 | 0.550 |
MOD_CK1_1 | 211 | 217 | PF00069 | 0.454 |
MOD_CK1_1 | 325 | 331 | PF00069 | 0.422 |
MOD_CK1_1 | 367 | 373 | PF00069 | 0.537 |
MOD_CK1_1 | 458 | 464 | PF00069 | 0.506 |
MOD_CK1_1 | 495 | 501 | PF00069 | 0.510 |
MOD_CK1_1 | 548 | 554 | PF00069 | 0.754 |
MOD_CK1_1 | 56 | 62 | PF00069 | 0.487 |
MOD_CK1_1 | 9 | 15 | PF00069 | 0.488 |
MOD_CK2_1 | 314 | 320 | PF00069 | 0.492 |
MOD_CK2_1 | 449 | 455 | PF00069 | 0.467 |
MOD_CK2_1 | 49 | 55 | PF00069 | 0.475 |
MOD_CK2_1 | 56 | 62 | PF00069 | 0.496 |
MOD_CK2_1 | 75 | 81 | PF00069 | 0.248 |
MOD_Cter_Amidation | 140 | 143 | PF01082 | 0.485 |
MOD_Cter_Amidation | 569 | 572 | PF01082 | 0.754 |
MOD_GlcNHglycan | 102 | 105 | PF01048 | 0.635 |
MOD_GlcNHglycan | 144 | 147 | PF01048 | 0.533 |
MOD_GlcNHglycan | 213 | 216 | PF01048 | 0.438 |
MOD_GlcNHglycan | 244 | 247 | PF01048 | 0.360 |
MOD_GlcNHglycan | 345 | 348 | PF01048 | 0.314 |
MOD_GlcNHglycan | 360 | 363 | PF01048 | 0.337 |
MOD_GlcNHglycan | 415 | 418 | PF01048 | 0.537 |
MOD_GlcNHglycan | 542 | 545 | PF01048 | 0.598 |
MOD_GlcNHglycan | 560 | 563 | PF01048 | 0.721 |
MOD_GlcNHglycan | 9 | 12 | PF01048 | 0.533 |
MOD_GlcNHglycan | 98 | 101 | PF01048 | 0.606 |
MOD_GSK3_1 | 104 | 111 | PF00069 | 0.657 |
MOD_GSK3_1 | 122 | 129 | PF00069 | 0.459 |
MOD_GSK3_1 | 382 | 389 | PF00069 | 0.719 |
MOD_GSK3_1 | 397 | 404 | PF00069 | 0.600 |
MOD_GSK3_1 | 413 | 420 | PF00069 | 0.429 |
MOD_GSK3_1 | 445 | 452 | PF00069 | 0.440 |
MOD_GSK3_1 | 45 | 52 | PF00069 | 0.486 |
MOD_GSK3_1 | 540 | 547 | PF00069 | 0.574 |
MOD_GSK3_1 | 602 | 609 | PF00069 | 0.684 |
MOD_GSK3_1 | 75 | 82 | PF00069 | 0.477 |
MOD_GSK3_1 | 96 | 103 | PF00069 | 0.593 |
MOD_N-GLC_1 | 242 | 247 | PF02516 | 0.337 |
MOD_N-GLC_1 | 343 | 348 | PF02516 | 0.310 |
MOD_NEK2_1 | 128 | 133 | PF00069 | 0.532 |
MOD_NEK2_1 | 257 | 262 | PF00069 | 0.470 |
MOD_NEK2_1 | 343 | 348 | PF00069 | 0.499 |
MOD_NEK2_1 | 383 | 388 | PF00069 | 0.590 |
MOD_NEK2_1 | 430 | 435 | PF00069 | 0.483 |
MOD_NEK2_1 | 49 | 54 | PF00069 | 0.449 |
MOD_NEK2_1 | 602 | 607 | PF00069 | 0.463 |
MOD_NEK2_1 | 7 | 12 | PF00069 | 0.442 |
MOD_NEK2_1 | 79 | 84 | PF00069 | 0.447 |
MOD_NEK2_2 | 75 | 80 | PF00069 | 0.472 |
MOD_PKA_1 | 142 | 148 | PF00069 | 0.489 |
MOD_PKA_1 | 571 | 577 | PF00069 | 0.671 |
MOD_PKA_2 | 470 | 476 | PF00069 | 0.425 |
MOD_PKA_2 | 495 | 501 | PF00069 | 0.529 |
MOD_PKB_1 | 380 | 388 | PF00069 | 0.628 |
MOD_PKB_1 | 569 | 577 | PF00069 | 0.721 |
MOD_Plk_1 | 123 | 129 | PF00069 | 0.519 |
MOD_Plk_1 | 235 | 241 | PF00069 | 0.510 |
MOD_Plk_1 | 343 | 349 | PF00069 | 0.495 |
MOD_Plk_4 | 235 | 241 | PF00069 | 0.501 |
MOD_Plk_4 | 259 | 265 | PF00069 | 0.472 |
MOD_Plk_4 | 322 | 328 | PF00069 | 0.431 |
MOD_Plk_4 | 364 | 370 | PF00069 | 0.530 |
MOD_Plk_4 | 430 | 436 | PF00069 | 0.386 |
MOD_Plk_4 | 439 | 445 | PF00069 | 0.354 |
MOD_Plk_4 | 45 | 51 | PF00069 | 0.506 |
MOD_Plk_4 | 460 | 466 | PF00069 | 0.429 |
MOD_Plk_4 | 75 | 81 | PF00069 | 0.480 |
MOD_ProDKin_1 | 108 | 114 | PF00069 | 0.692 |
MOD_ProDKin_1 | 291 | 297 | PF00069 | 0.537 |
MOD_ProDKin_1 | 501 | 507 | PF00069 | 0.633 |
MOD_ProDKin_1 | 53 | 59 | PF00069 | 0.506 |
MOD_ProDKin_1 | 546 | 552 | PF00069 | 0.690 |
MOD_SUMO_for_1 | 528 | 531 | PF00179 | 0.624 |
MOD_SUMO_rev_2 | 145 | 151 | PF00179 | 0.528 |
MOD_SUMO_rev_2 | 56 | 66 | PF00179 | 0.444 |
TRG_DiLeu_BaEn_1 | 68 | 73 | PF01217 | 0.433 |
TRG_DiLeu_BaEn_3 | 236 | 242 | PF01217 | 0.533 |
TRG_DiLeu_BaEn_4 | 318 | 324 | PF01217 | 0.528 |
TRG_DiLeu_BaLyEn_6 | 195 | 200 | PF01217 | 0.512 |
TRG_DiLeu_BaLyEn_6 | 476 | 481 | PF01217 | 0.438 |
TRG_ENDOCYTIC_2 | 175 | 178 | PF00928 | 0.437 |
TRG_ENDOCYTIC_2 | 254 | 257 | PF00928 | 0.500 |
TRG_ENDOCYTIC_2 | 3 | 6 | PF00928 | 0.472 |
TRG_ENDOCYTIC_2 | 434 | 437 | PF00928 | 0.420 |
TRG_ENDOCYTIC_2 | 77 | 80 | PF00928 | 0.371 |
TRG_ENDOCYTIC_2 | 90 | 93 | PF00928 | 0.428 |
TRG_ER_diArg_1 | 222 | 225 | PF00400 | 0.463 |
TRG_ER_diArg_1 | 301 | 303 | PF00400 | 0.537 |
TRG_ER_diArg_1 | 340 | 343 | PF00400 | 0.471 |
TRG_ER_diArg_1 | 379 | 382 | PF00400 | 0.502 |
TRG_ER_diArg_1 | 477 | 479 | PF00400 | 0.368 |
TRG_ER_diArg_1 | 568 | 571 | PF00400 | 0.721 |
TRG_Pf-PMV_PEXEL_1 | 509 | 513 | PF00026 | 0.542 |
TRG_Pf-PMV_PEXEL_1 | 64 | 68 | PF00026 | 0.482 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PAW4 | Leptomonas seymouri | 67% | 100% |
A0A0S4JG90 | Bodo saltans | 36% | 100% |
A0A1X0NLX9 | Trypanosomatidae | 43% | 100% |
A0A3S7WP82 | Leishmania donovani | 95% | 100% |
A0A422N510 | Trypanosoma rangeli | 45% | 100% |
A4H4E6 | Leishmania braziliensis | 84% | 99% |
A4HSM3 | Leishmania infantum | 95% | 100% |
E9AKK7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
Q05B63 | Bos taurus | 26% | 100% |
Q12463 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 26% | 100% |
Q54QA6 | Dictyostelium discoideum | 27% | 100% |
Q5R962 | Pongo abelii | 27% | 100% |
Q6NS23 | Xenopus laevis | 25% | 100% |
Q7TNK6 | Rattus norvegicus | 27% | 100% |
Q9CWH5 | Mus musculus | 26% | 100% |
V5B7D5 | Trypanosoma cruzi | 45% | 100% |