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:0005840 | ribosome | 5 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043228 | non-membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: A0A3S7WYR3
Term | Name | Level | Count |
---|---|---|---|
GO:0006412 | translation | 4 | 2 |
GO:0006518 | peptide metabolic process | 4 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0009058 | biosynthetic process | 2 | 2 |
GO:0009059 | macromolecule biosynthetic process | 4 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0019538 | protein metabolic process | 3 | 2 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 2 |
GO:0034645 | obsolete cellular macromolecule biosynthetic process | 4 | 2 |
GO:0043043 | peptide biosynthetic process | 5 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0043603 | amide metabolic process | 3 | 2 |
GO:0043604 | amide biosynthetic process | 4 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0044249 | cellular biosynthetic process | 3 | 2 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 2 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 2 |
GO:1901566 | organonitrogen compound biosynthetic process | 4 | 2 |
GO:1901576 | organic substance biosynthetic process | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003735 | structural constituent of ribosome | 2 | 2 |
GO:0005198 | structural molecule activity | 1 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 355 | 359 | PF00656 | 0.726 |
CLV_C14_Caspase3-7 | 502 | 506 | PF00656 | 0.494 |
CLV_NRD_NRD_1 | 342 | 344 | PF00675 | 0.845 |
CLV_NRD_NRD_1 | 364 | 366 | PF00675 | 0.673 |
CLV_NRD_NRD_1 | 423 | 425 | PF00675 | 0.629 |
CLV_NRD_NRD_1 | 457 | 459 | PF00675 | 0.684 |
CLV_NRD_NRD_1 | 562 | 564 | PF00675 | 0.718 |
CLV_NRD_NRD_1 | 573 | 575 | PF00675 | 0.397 |
CLV_PCSK_FUR_1 | 560 | 564 | PF00082 | 0.813 |
CLV_PCSK_FUR_1 | 571 | 575 | PF00082 | 0.417 |
CLV_PCSK_KEX2_1 | 248 | 250 | PF00082 | 0.855 |
CLV_PCSK_KEX2_1 | 342 | 344 | PF00082 | 0.772 |
CLV_PCSK_KEX2_1 | 423 | 425 | PF00082 | 0.629 |
CLV_PCSK_KEX2_1 | 457 | 459 | PF00082 | 0.684 |
CLV_PCSK_KEX2_1 | 562 | 564 | PF00082 | 0.718 |
CLV_PCSK_KEX2_1 | 573 | 575 | PF00082 | 0.397 |
CLV_PCSK_PC1ET2_1 | 248 | 250 | PF00082 | 0.855 |
CLV_PCSK_PC7_1 | 338 | 344 | PF00082 | 0.724 |
CLV_PCSK_PC7_1 | 419 | 425 | PF00082 | 0.707 |
CLV_PCSK_SKI1_1 | 119 | 123 | PF00082 | 0.649 |
CLV_PCSK_SKI1_1 | 129 | 133 | PF00082 | 0.542 |
CLV_PCSK_SKI1_1 | 372 | 376 | PF00082 | 0.578 |
CLV_PCSK_SKI1_1 | 585 | 589 | PF00082 | 0.591 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.756 |
DEG_SCF_FBW7_2 | 300 | 306 | PF00400 | 0.755 |
DEG_SPOP_SBC_1 | 152 | 156 | PF00917 | 0.695 |
DEG_SPOP_SBC_1 | 609 | 613 | PF00917 | 0.686 |
DOC_CKS1_1 | 265 | 270 | PF01111 | 0.717 |
DOC_CKS1_1 | 300 | 305 | PF01111 | 0.752 |
DOC_CKS1_1 | 427 | 432 | PF01111 | 0.687 |
DOC_CYCLIN_yCln2_LP_2 | 265 | 271 | PF00134 | 0.783 |
DOC_CYCLIN_yCln2_LP_2 | 525 | 531 | PF00134 | 0.461 |
DOC_MAPK_DCC_7 | 661 | 671 | PF00069 | 0.487 |
DOC_MAPK_gen_1 | 127 | 134 | PF00069 | 0.684 |
DOC_MAPK_gen_1 | 571 | 580 | PF00069 | 0.572 |
DOC_MAPK_MEF2A_6 | 571 | 580 | PF00069 | 0.572 |
DOC_PP1_RVXF_1 | 476 | 483 | PF00149 | 0.545 |
DOC_PP2B_LxvP_1 | 400 | 403 | PF13499 | 0.682 |
DOC_PP2B_LxvP_1 | 525 | 528 | PF13499 | 0.489 |
DOC_USP7_MATH_1 | 103 | 107 | PF00917 | 0.735 |
DOC_USP7_MATH_1 | 110 | 114 | PF00917 | 0.582 |
DOC_USP7_MATH_1 | 152 | 156 | PF00917 | 0.641 |
DOC_USP7_MATH_1 | 22 | 26 | PF00917 | 0.758 |
DOC_USP7_MATH_1 | 244 | 248 | PF00917 | 0.704 |
DOC_USP7_MATH_1 | 255 | 259 | PF00917 | 0.788 |
DOC_USP7_MATH_1 | 276 | 280 | PF00917 | 0.822 |
DOC_USP7_MATH_1 | 285 | 289 | PF00917 | 0.745 |
DOC_USP7_MATH_1 | 293 | 297 | PF00917 | 0.650 |
DOC_USP7_MATH_1 | 307 | 311 | PF00917 | 0.779 |
DOC_USP7_MATH_1 | 325 | 329 | PF00917 | 0.624 |
DOC_USP7_MATH_1 | 411 | 415 | PF00917 | 0.651 |
DOC_USP7_MATH_1 | 439 | 443 | PF00917 | 0.641 |
DOC_USP7_MATH_1 | 77 | 81 | PF00917 | 0.668 |
DOC_USP7_MATH_1 | 86 | 90 | PF00917 | 0.760 |
DOC_WW_Pin1_4 | 148 | 153 | PF00397 | 0.670 |
DOC_WW_Pin1_4 | 166 | 171 | PF00397 | 0.496 |
DOC_WW_Pin1_4 | 18 | 23 | PF00397 | 0.780 |
DOC_WW_Pin1_4 | 186 | 191 | PF00397 | 0.663 |
DOC_WW_Pin1_4 | 213 | 218 | PF00397 | 0.670 |
DOC_WW_Pin1_4 | 259 | 264 | PF00397 | 0.805 |
DOC_WW_Pin1_4 | 279 | 284 | PF00397 | 0.600 |
DOC_WW_Pin1_4 | 287 | 292 | PF00397 | 0.700 |
DOC_WW_Pin1_4 | 29 | 34 | PF00397 | 0.627 |
DOC_WW_Pin1_4 | 294 | 299 | PF00397 | 0.689 |
DOC_WW_Pin1_4 | 326 | 331 | PF00397 | 0.776 |
DOC_WW_Pin1_4 | 348 | 353 | PF00397 | 0.718 |
DOC_WW_Pin1_4 | 360 | 365 | PF00397 | 0.722 |
DOC_WW_Pin1_4 | 426 | 431 | PF00397 | 0.648 |
DOC_WW_Pin1_4 | 433 | 438 | PF00397 | 0.636 |
DOC_WW_Pin1_4 | 441 | 446 | PF00397 | 0.691 |
DOC_WW_Pin1_4 | 47 | 52 | PF00397 | 0.609 |
DOC_WW_Pin1_4 | 547 | 552 | PF00397 | 0.515 |
LIG_14-3-3_CanoR_1 | 159 | 165 | PF00244 | 0.747 |
LIG_14-3-3_CanoR_1 | 204 | 209 | PF00244 | 0.840 |
LIG_14-3-3_CanoR_1 | 324 | 330 | PF00244 | 0.739 |
LIG_14-3-3_CanoR_1 | 342 | 350 | PF00244 | 0.643 |
LIG_14-3-3_CanoR_1 | 365 | 374 | PF00244 | 0.789 |
LIG_14-3-3_CanoR_1 | 424 | 430 | PF00244 | 0.724 |
LIG_14-3-3_CanoR_1 | 539 | 545 | PF00244 | 0.550 |
LIG_BIR_III_4 | 238 | 242 | PF00653 | 0.652 |
LIG_BRCT_BRCA1_1 | 540 | 544 | PF00533 | 0.387 |
LIG_EVH1_2 | 260 | 264 | PF00568 | 0.618 |
LIG_FHA_1 | 404 | 410 | PF00498 | 0.702 |
LIG_FHA_1 | 427 | 433 | PF00498 | 0.641 |
LIG_FHA_1 | 448 | 454 | PF00498 | 0.673 |
LIG_FHA_1 | 48 | 54 | PF00498 | 0.663 |
LIG_FHA_1 | 502 | 508 | PF00498 | 0.462 |
LIG_FHA_1 | 600 | 606 | PF00498 | 0.466 |
LIG_IBAR_NPY_1 | 90 | 92 | PF08397 | 0.794 |
LIG_KLC1_Yacidic_2 | 643 | 647 | PF13176 | 0.556 |
LIG_LIR_Apic_2 | 462 | 468 | PF02991 | 0.615 |
LIG_LIR_Apic_2 | 618 | 624 | PF02991 | 0.557 |
LIG_LIR_Apic_2 | 96 | 100 | PF02991 | 0.786 |
LIG_LIR_Nem_3 | 584 | 590 | PF02991 | 0.488 |
LIG_NRBOX | 677 | 683 | PF00104 | 0.371 |
LIG_PDZ_Class_2 | 680 | 685 | PF00595 | 0.483 |
LIG_Pex14_2 | 544 | 548 | PF04695 | 0.464 |
LIG_PTAP_UEV_1 | 256 | 261 | PF05743 | 0.623 |
LIG_SH2_CRK | 54 | 58 | PF00017 | 0.791 |
LIG_SH2_CRK | 621 | 625 | PF00017 | 0.618 |
LIG_SH2_SRC | 465 | 468 | PF00017 | 0.692 |
LIG_SH2_SRC | 625 | 628 | PF00017 | 0.608 |
LIG_SH2_SRC | 645 | 648 | PF00017 | 0.576 |
LIG_SH2_STAP1 | 45 | 49 | PF00017 | 0.751 |
LIG_SH2_STAT5 | 229 | 232 | PF00017 | 0.818 |
LIG_SH2_STAT5 | 45 | 48 | PF00017 | 0.752 |
LIG_SH2_STAT5 | 497 | 500 | PF00017 | 0.395 |
LIG_SH2_STAT5 | 599 | 602 | PF00017 | 0.468 |
LIG_SH2_STAT5 | 645 | 648 | PF00017 | 0.576 |
LIG_SH2_STAT5 | 67 | 70 | PF00017 | 0.755 |
LIG_SH2_STAT5 | 72 | 75 | PF00017 | 0.732 |
LIG_SH2_STAT5 | 92 | 95 | PF00017 | 0.734 |
LIG_SH3_1 | 347 | 353 | PF00018 | 0.778 |
LIG_SH3_1 | 361 | 367 | PF00018 | 0.556 |
LIG_SH3_1 | 465 | 471 | PF00018 | 0.571 |
LIG_SH3_1 | 621 | 627 | PF00018 | 0.616 |
LIG_SH3_2 | 100 | 105 | PF14604 | 0.673 |
LIG_SH3_2 | 300 | 305 | PF14604 | 0.752 |
LIG_SH3_3 | 159 | 165 | PF00018 | 0.687 |
LIG_SH3_3 | 208 | 214 | PF00018 | 0.733 |
LIG_SH3_3 | 251 | 257 | PF00018 | 0.751 |
LIG_SH3_3 | 297 | 303 | PF00018 | 0.699 |
LIG_SH3_3 | 347 | 353 | PF00018 | 0.778 |
LIG_SH3_3 | 361 | 367 | PF00018 | 0.556 |
LIG_SH3_3 | 435 | 441 | PF00018 | 0.784 |
LIG_SH3_3 | 465 | 471 | PF00018 | 0.603 |
LIG_SH3_3 | 621 | 627 | PF00018 | 0.616 |
LIG_SH3_3 | 662 | 668 | PF00018 | 0.436 |
LIG_SH3_3 | 80 | 86 | PF00018 | 0.667 |
LIG_SH3_3 | 97 | 103 | PF00018 | 0.784 |
LIG_SUMO_SIM_anti_2 | 504 | 511 | PF11976 | 0.619 |
LIG_SUMO_SIM_par_1 | 667 | 673 | PF11976 | 0.443 |
LIG_SxIP_EBH_1 | 19 | 33 | PF03271 | 0.804 |
MOD_CDC14_SPxK_1 | 292 | 295 | PF00782 | 0.751 |
MOD_CDC14_SPxK_1 | 331 | 334 | PF00782 | 0.831 |
MOD_CDC14_SPxK_1 | 34 | 37 | PF00782 | 0.684 |
MOD_CDC14_SPxK_1 | 363 | 366 | PF00782 | 0.780 |
MOD_CDK_SPK_2 | 360 | 365 | PF00069 | 0.766 |
MOD_CDK_SPxK_1 | 289 | 295 | PF00069 | 0.754 |
MOD_CDK_SPxK_1 | 299 | 305 | PF00069 | 0.712 |
MOD_CDK_SPxK_1 | 31 | 37 | PF00069 | 0.687 |
MOD_CDK_SPxK_1 | 328 | 334 | PF00069 | 0.826 |
MOD_CDK_SPxK_1 | 360 | 366 | PF00069 | 0.786 |
MOD_CDK_SPxxK_3 | 441 | 448 | PF00069 | 0.684 |
MOD_CK1_1 | 151 | 157 | PF00069 | 0.770 |
MOD_CK1_1 | 184 | 190 | PF00069 | 0.765 |
MOD_CK1_1 | 215 | 221 | PF00069 | 0.739 |
MOD_CK1_1 | 279 | 285 | PF00069 | 0.649 |
MOD_CK1_1 | 310 | 316 | PF00069 | 0.731 |
MOD_CK1_1 | 328 | 334 | PF00069 | 0.715 |
MOD_CK1_1 | 360 | 366 | PF00069 | 0.795 |
MOD_CK1_1 | 461 | 467 | PF00069 | 0.639 |
MOD_CK1_1 | 55 | 61 | PF00069 | 0.720 |
MOD_CK1_1 | 550 | 556 | PF00069 | 0.586 |
MOD_CK1_1 | 610 | 616 | PF00069 | 0.651 |
MOD_CK1_1 | 75 | 81 | PF00069 | 0.467 |
MOD_CK1_1 | 9 | 15 | PF00069 | 0.668 |
MOD_CK2_1 | 120 | 126 | PF00069 | 0.535 |
MOD_CK2_1 | 309 | 315 | PF00069 | 0.753 |
MOD_CK2_1 | 41 | 47 | PF00069 | 0.724 |
MOD_GlcNHglycan | 105 | 108 | PF01048 | 0.801 |
MOD_GlcNHglycan | 112 | 115 | PF01048 | 0.646 |
MOD_GlcNHglycan | 155 | 158 | PF01048 | 0.776 |
MOD_GlcNHglycan | 220 | 223 | PF01048 | 0.734 |
MOD_GlcNHglycan | 24 | 27 | PF01048 | 0.769 |
MOD_GlcNHglycan | 256 | 260 | PF01048 | 0.716 |
MOD_GlcNHglycan | 278 | 281 | PF01048 | 0.781 |
MOD_GlcNHglycan | 29 | 32 | PF01048 | 0.725 |
MOD_GlcNHglycan | 318 | 321 | PF01048 | 0.811 |
MOD_GlcNHglycan | 368 | 371 | PF01048 | 0.770 |
MOD_GlcNHglycan | 38 | 42 | PF01048 | 0.608 |
MOD_GlcNHglycan | 403 | 406 | PF01048 | 0.709 |
MOD_GlcNHglycan | 486 | 489 | PF01048 | 0.480 |
MOD_GlcNHglycan | 54 | 57 | PF01048 | 0.707 |
MOD_GlcNHglycan | 557 | 560 | PF01048 | 0.721 |
MOD_GlcNHglycan | 59 | 62 | PF01048 | 0.734 |
MOD_GlcNHglycan | 613 | 616 | PF01048 | 0.658 |
MOD_GlcNHglycan | 64 | 67 | PF01048 | 0.661 |
MOD_GlcNHglycan | 672 | 675 | PF01048 | 0.576 |
MOD_GlcNHglycan | 74 | 77 | PF01048 | 0.460 |
MOD_GlcNHglycan | 8 | 11 | PF01048 | 0.664 |
MOD_GSK3_1 | 148 | 155 | PF00069 | 0.640 |
MOD_GSK3_1 | 18 | 25 | PF00069 | 0.760 |
MOD_GSK3_1 | 181 | 188 | PF00069 | 0.699 |
MOD_GSK3_1 | 255 | 262 | PF00069 | 0.809 |
MOD_GSK3_1 | 27 | 34 | PF00069 | 0.622 |
MOD_GSK3_1 | 285 | 292 | PF00069 | 0.738 |
MOD_GSK3_1 | 307 | 314 | PF00069 | 0.738 |
MOD_GSK3_1 | 316 | 323 | PF00069 | 0.703 |
MOD_GSK3_1 | 348 | 355 | PF00069 | 0.748 |
MOD_GSK3_1 | 37 | 44 | PF00069 | 0.618 |
MOD_GSK3_1 | 55 | 62 | PF00069 | 0.588 |
MOD_GSK3_1 | 581 | 588 | PF00069 | 0.465 |
MOD_GSK3_1 | 607 | 614 | PF00069 | 0.565 |
MOD_GSK3_1 | 71 | 78 | PF00069 | 0.610 |
MOD_GSK3_1 | 86 | 93 | PF00069 | 0.713 |
MOD_NEK2_1 | 153 | 158 | PF00069 | 0.663 |
MOD_NEK2_1 | 160 | 165 | PF00069 | 0.725 |
MOD_NEK2_1 | 409 | 414 | PF00069 | 0.682 |
MOD_NEK2_1 | 432 | 437 | PF00069 | 0.721 |
MOD_NEK2_1 | 535 | 540 | PF00069 | 0.465 |
MOD_NEK2_1 | 57 | 62 | PF00069 | 0.760 |
MOD_NEK2_1 | 598 | 603 | PF00069 | 0.408 |
MOD_PIKK_1 | 342 | 348 | PF00454 | 0.633 |
MOD_PKA_1 | 342 | 348 | PF00069 | 0.633 |
MOD_PKA_2 | 158 | 164 | PF00069 | 0.745 |
MOD_PKA_2 | 341 | 347 | PF00069 | 0.747 |
MOD_PKA_2 | 425 | 431 | PF00069 | 0.780 |
MOD_PKA_2 | 447 | 453 | PF00069 | 0.736 |
MOD_PKA_2 | 538 | 544 | PF00069 | 0.397 |
MOD_PKA_2 | 555 | 561 | PF00069 | 0.704 |
MOD_Plk_1 | 176 | 182 | PF00069 | 0.763 |
MOD_Plk_1 | 37 | 43 | PF00069 | 0.732 |
MOD_ProDKin_1 | 148 | 154 | PF00069 | 0.675 |
MOD_ProDKin_1 | 166 | 172 | PF00069 | 0.495 |
MOD_ProDKin_1 | 18 | 24 | PF00069 | 0.779 |
MOD_ProDKin_1 | 186 | 192 | PF00069 | 0.663 |
MOD_ProDKin_1 | 213 | 219 | PF00069 | 0.670 |
MOD_ProDKin_1 | 259 | 265 | PF00069 | 0.808 |
MOD_ProDKin_1 | 279 | 285 | PF00069 | 0.593 |
MOD_ProDKin_1 | 287 | 293 | PF00069 | 0.701 |
MOD_ProDKin_1 | 29 | 35 | PF00069 | 0.622 |
MOD_ProDKin_1 | 294 | 300 | PF00069 | 0.686 |
MOD_ProDKin_1 | 326 | 332 | PF00069 | 0.770 |
MOD_ProDKin_1 | 348 | 354 | PF00069 | 0.716 |
MOD_ProDKin_1 | 360 | 366 | PF00069 | 0.721 |
MOD_ProDKin_1 | 426 | 432 | PF00069 | 0.652 |
MOD_ProDKin_1 | 433 | 439 | PF00069 | 0.637 |
MOD_ProDKin_1 | 441 | 447 | PF00069 | 0.693 |
MOD_ProDKin_1 | 47 | 53 | PF00069 | 0.610 |
MOD_ProDKin_1 | 547 | 553 | PF00069 | 0.529 |
TRG_DiLeu_BaEn_2 | 592 | 598 | PF01217 | 0.485 |
TRG_ENDOCYTIC_2 | 54 | 57 | PF00928 | 0.791 |
TRG_ER_diArg_1 | 143 | 146 | PF00400 | 0.595 |
TRG_ER_diArg_1 | 423 | 425 | PF00400 | 0.594 |
TRG_ER_diArg_1 | 456 | 458 | PF00400 | 0.711 |
TRG_ER_diArg_1 | 560 | 563 | PF00400 | 0.718 |
TRG_ER_diArg_1 | 571 | 574 | PF00400 | 0.424 |
TRG_Pf-PMV_PEXEL_1 | 129 | 133 | PF00026 | 0.684 |
TRG_Pf-PMV_PEXEL_1 | 136 | 140 | PF00026 | 0.564 |
TRG_Pf-PMV_PEXEL_1 | 478 | 483 | PF00026 | 0.483 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7X1 | Leptomonas seymouri | 41% | 95% |
A4HDY0 | Leishmania braziliensis | 71% | 100% |
A4I176 | Leishmania infantum | 100% | 100% |
E9AXB0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
Q4QA62 | Leishmania major | 89% | 100% |