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 | 1 |
GO:0031974 | membrane-enclosed lumen | 2 | 1 |
GO:0031981 | nuclear lumen | 5 | 1 |
GO:0032838 | plasma membrane bounded cell projection cytoplasm | 4 | 1 |
GO:0043233 | organelle lumen | 3 | 1 |
GO:0070013 | intracellular organelle lumen | 4 | 1 |
GO:0097014 | ciliary plasm | 5 | 1 |
GO:0099568 | cytoplasmic region | 3 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A0A3S5H5B1
Term | Name | Level | Count |
---|---|---|---|
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0016567 | protein ubiquitination | 7 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0032446 | protein modification by small protein conjugation | 6 | 1 |
GO:0036211 | protein modification process | 4 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0070647 | protein modification by small protein conjugation or removal | 5 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 11 |
GO:0005509 | calcium ion binding | 5 | 10 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043169 | cation binding | 3 | 11 |
GO:0046872 | metal ion binding | 4 | 11 |
GO:0003824 | catalytic activity | 1 | 1 |
GO:0004842 | ubiquitin-protein transferase activity | 4 | 1 |
GO:0016740 | transferase activity | 2 | 1 |
GO:0019787 | ubiquitin-like protein transferase activity | 3 | 1 |
GO:0061630 | ubiquitin protein ligase activity | 5 | 1 |
GO:0061659 | ubiquitin-like protein ligase activity | 4 | 1 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 115 | 119 | PF00656 | 0.450 |
CLV_C14_Caspase3-7 | 347 | 351 | PF00656 | 0.387 |
CLV_NRD_NRD_1 | 170 | 172 | PF00675 | 0.597 |
CLV_NRD_NRD_1 | 259 | 261 | PF00675 | 0.449 |
CLV_NRD_NRD_1 | 460 | 462 | PF00675 | 0.568 |
CLV_PCSK_KEX2_1 | 170 | 172 | PF00082 | 0.571 |
CLV_PCSK_KEX2_1 | 259 | 261 | PF00082 | 0.449 |
CLV_PCSK_KEX2_1 | 46 | 48 | PF00082 | 0.252 |
CLV_PCSK_KEX2_1 | 460 | 462 | PF00082 | 0.561 |
CLV_PCSK_PC1ET2_1 | 46 | 48 | PF00082 | 0.252 |
CLV_PCSK_PC7_1 | 166 | 172 | PF00082 | 0.545 |
CLV_PCSK_SKI1_1 | 405 | 409 | PF00082 | 0.372 |
CLV_PCSK_SKI1_1 | 412 | 416 | PF00082 | 0.373 |
CLV_PCSK_SKI1_1 | 8 | 12 | PF00082 | 0.377 |
CLV_PCSK_SKI1_1 | 83 | 87 | PF00082 | 0.458 |
DEG_APCC_DBOX_1 | 259 | 267 | PF00400 | 0.388 |
DEG_APCC_DBOX_1 | 404 | 412 | PF00400 | 0.329 |
DEG_APCC_DBOX_1 | 82 | 90 | PF00400 | 0.394 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.477 |
DEG_SPOP_SBC_1 | 433 | 437 | PF00917 | 0.535 |
DEG_SPOP_SBC_1 | 450 | 454 | PF00917 | 0.505 |
DOC_CKS1_1 | 228 | 233 | PF01111 | 0.553 |
DOC_CKS1_1 | 422 | 427 | PF01111 | 0.457 |
DOC_CYCLIN_RxL_1 | 79 | 88 | PF00134 | 0.405 |
DOC_MAPK_gen_1 | 79 | 86 | PF00069 | 0.362 |
DOC_MAPK_MEF2A_6 | 302 | 310 | PF00069 | 0.345 |
DOC_PP1_RVXF_1 | 289 | 296 | PF00149 | 0.399 |
DOC_PP2B_LxvP_1 | 525 | 528 | PF13499 | 0.567 |
DOC_PP2B_PxIxI_1 | 426 | 432 | PF00149 | 0.512 |
DOC_PP4_FxxP_1 | 22 | 25 | PF00568 | 0.337 |
DOC_PP4_FxxP_1 | 66 | 69 | PF00568 | 0.295 |
DOC_USP7_MATH_1 | 120 | 124 | PF00917 | 0.507 |
DOC_USP7_MATH_1 | 249 | 253 | PF00917 | 0.610 |
DOC_USP7_MATH_1 | 335 | 339 | PF00917 | 0.411 |
DOC_USP7_MATH_1 | 450 | 454 | PF00917 | 0.549 |
DOC_USP7_MATH_1 | 462 | 466 | PF00917 | 0.525 |
DOC_USP7_MATH_1 | 494 | 498 | PF00917 | 0.527 |
DOC_USP7_MATH_2 | 212 | 218 | PF00917 | 0.538 |
DOC_WW_Pin1_4 | 137 | 142 | PF00397 | 0.591 |
DOC_WW_Pin1_4 | 152 | 157 | PF00397 | 0.608 |
DOC_WW_Pin1_4 | 159 | 164 | PF00397 | 0.561 |
DOC_WW_Pin1_4 | 195 | 200 | PF00397 | 0.574 |
DOC_WW_Pin1_4 | 223 | 228 | PF00397 | 0.582 |
DOC_WW_Pin1_4 | 247 | 252 | PF00397 | 0.571 |
DOC_WW_Pin1_4 | 380 | 385 | PF00397 | 0.337 |
DOC_WW_Pin1_4 | 421 | 426 | PF00397 | 0.460 |
DOC_WW_Pin1_4 | 451 | 456 | PF00397 | 0.606 |
DOC_WW_Pin1_4 | 520 | 525 | PF00397 | 0.639 |
DOC_WW_Pin1_4 | 550 | 555 | PF00397 | 0.522 |
DOC_WW_Pin1_4 | 561 | 566 | PF00397 | 0.532 |
LIG_14-3-3_CanoR_1 | 193 | 200 | PF00244 | 0.576 |
LIG_14-3-3_CanoR_1 | 260 | 268 | PF00244 | 0.475 |
LIG_14-3-3_CanoR_1 | 284 | 290 | PF00244 | 0.306 |
LIG_14-3-3_CanoR_1 | 328 | 334 | PF00244 | 0.409 |
LIG_14-3-3_CanoR_1 | 8 | 13 | PF00244 | 0.369 |
LIG_BIR_III_4 | 367 | 371 | PF00653 | 0.273 |
LIG_BRCT_BRCA1_1 | 337 | 341 | PF00533 | 0.409 |
LIG_BRCT_BRCA1_1 | 485 | 489 | PF00533 | 0.545 |
LIG_CtBP_PxDLS_1 | 34 | 38 | PF00389 | 0.272 |
LIG_FHA_1 | 223 | 229 | PF00498 | 0.580 |
LIG_FHA_1 | 347 | 353 | PF00498 | 0.373 |
LIG_FHA_1 | 397 | 403 | PF00498 | 0.377 |
LIG_FHA_2 | 113 | 119 | PF00498 | 0.490 |
LIG_FHA_2 | 138 | 144 | PF00498 | 0.538 |
LIG_FHA_2 | 414 | 420 | PF00498 | 0.406 |
LIG_Integrin_isoDGR_2 | 579 | 581 | PF01839 | 0.569 |
LIG_Integrin_RGD_1 | 584 | 586 | PF01839 | 0.524 |
LIG_LIR_Apic_2 | 19 | 25 | PF02991 | 0.363 |
LIG_LIR_Apic_2 | 29 | 34 | PF02991 | 0.302 |
LIG_LIR_Gen_1 | 267 | 276 | PF02991 | 0.413 |
LIG_LIR_Gen_1 | 399 | 408 | PF02991 | 0.411 |
LIG_LIR_Gen_1 | 512 | 522 | PF02991 | 0.542 |
LIG_LIR_Nem_3 | 177 | 183 | PF02991 | 0.604 |
LIG_LIR_Nem_3 | 256 | 261 | PF02991 | 0.427 |
LIG_LIR_Nem_3 | 267 | 271 | PF02991 | 0.458 |
LIG_LIR_Nem_3 | 359 | 365 | PF02991 | 0.423 |
LIG_LIR_Nem_3 | 369 | 374 | PF02991 | 0.362 |
LIG_LIR_Nem_3 | 399 | 404 | PF02991 | 0.413 |
LIG_LIR_Nem_3 | 512 | 517 | PF02991 | 0.544 |
LIG_Pex14_2 | 295 | 299 | PF04695 | 0.371 |
LIG_Rb_pABgroove_1 | 272 | 280 | PF01858 | 0.369 |
LIG_SH2_CRK | 268 | 272 | PF00017 | 0.388 |
LIG_SH2_CRK | 362 | 366 | PF00017 | 0.512 |
LIG_SH2_CRK | 501 | 505 | PF00017 | 0.663 |
LIG_SH2_CRK | 514 | 518 | PF00017 | 0.563 |
LIG_SH2_PTP2 | 180 | 183 | PF00017 | 0.574 |
LIG_SH2_PTP2 | 401 | 404 | PF00017 | 0.353 |
LIG_SH2_SRC | 180 | 183 | PF00017 | 0.574 |
LIG_SH2_STAP1 | 268 | 272 | PF00017 | 0.388 |
LIG_SH2_STAP1 | 348 | 352 | PF00017 | 0.401 |
LIG_SH2_STAP1 | 514 | 518 | PF00017 | 0.549 |
LIG_SH2_STAT3 | 320 | 323 | PF00017 | 0.339 |
LIG_SH2_STAT5 | 180 | 183 | PF00017 | 0.581 |
LIG_SH2_STAT5 | 320 | 323 | PF00017 | 0.347 |
LIG_SH2_STAT5 | 348 | 351 | PF00017 | 0.395 |
LIG_SH2_STAT5 | 373 | 376 | PF00017 | 0.352 |
LIG_SH2_STAT5 | 401 | 404 | PF00017 | 0.353 |
LIG_SH2_STAT5 | 501 | 504 | PF00017 | 0.528 |
LIG_SH2_STAT5 | 98 | 101 | PF00017 | 0.383 |
LIG_SH3_2 | 521 | 526 | PF14604 | 0.562 |
LIG_SH3_3 | 153 | 159 | PF00018 | 0.618 |
LIG_SH3_3 | 331 | 337 | PF00018 | 0.352 |
LIG_SH3_3 | 444 | 450 | PF00018 | 0.502 |
LIG_SH3_3 | 518 | 524 | PF00018 | 0.678 |
LIG_SUMO_SIM_anti_2 | 33 | 39 | PF11976 | 0.282 |
LIG_SUMO_SIM_par_1 | 88 | 93 | PF11976 | 0.331 |
LIG_TRAF2_2 | 14 | 19 | PF00917 | 0.389 |
LIG_TYR_ITIM | 266 | 271 | PF00017 | 0.363 |
LIG_UBA3_1 | 309 | 318 | PF00899 | 0.365 |
MOD_CAAXbox | 589 | 592 | PF01239 | 0.588 |
MOD_CDC14_SPxK_1 | 198 | 201 | PF00782 | 0.557 |
MOD_CDC14_SPxK_1 | 523 | 526 | PF00782 | 0.553 |
MOD_CDK_SPxK_1 | 195 | 201 | PF00069 | 0.570 |
MOD_CDK_SPxK_1 | 520 | 526 | PF00069 | 0.546 |
MOD_CDK_SPxxK_3 | 159 | 166 | PF00069 | 0.547 |
MOD_CDK_SPxxK_3 | 561 | 568 | PF00069 | 0.570 |
MOD_CK1_1 | 136 | 142 | PF00069 | 0.594 |
MOD_CK1_1 | 188 | 194 | PF00069 | 0.622 |
MOD_CK1_1 | 195 | 201 | PF00069 | 0.616 |
MOD_CK1_1 | 217 | 223 | PF00069 | 0.736 |
MOD_CK1_1 | 413 | 419 | PF00069 | 0.468 |
MOD_CK1_1 | 434 | 440 | PF00069 | 0.753 |
MOD_CK1_1 | 472 | 478 | PF00069 | 0.522 |
MOD_CK1_1 | 512 | 518 | PF00069 | 0.515 |
MOD_CK2_1 | 137 | 143 | PF00069 | 0.533 |
MOD_CK2_1 | 261 | 267 | PF00069 | 0.368 |
MOD_CK2_1 | 341 | 347 | PF00069 | 0.387 |
MOD_CK2_1 | 413 | 419 | PF00069 | 0.394 |
MOD_GlcNHglycan | 188 | 191 | PF01048 | 0.624 |
MOD_GlcNHglycan | 238 | 241 | PF01048 | 0.591 |
MOD_GlcNHglycan | 247 | 250 | PF01048 | 0.491 |
MOD_GlcNHglycan | 285 | 288 | PF01048 | 0.345 |
MOD_GlcNHglycan | 336 | 340 | PF01048 | 0.411 |
MOD_GlcNHglycan | 367 | 371 | PF01048 | 0.273 |
MOD_GlcNHglycan | 438 | 441 | PF01048 | 0.631 |
MOD_GlcNHglycan | 474 | 477 | PF01048 | 0.575 |
MOD_GlcNHglycan | 479 | 482 | PF01048 | 0.530 |
MOD_GlcNHglycan | 541 | 544 | PF01048 | 0.596 |
MOD_GSK3_1 | 101 | 108 | PF00069 | 0.391 |
MOD_GSK3_1 | 120 | 127 | PF00069 | 0.582 |
MOD_GSK3_1 | 133 | 140 | PF00069 | 0.556 |
MOD_GSK3_1 | 154 | 161 | PF00069 | 0.671 |
MOD_GSK3_1 | 188 | 195 | PF00069 | 0.616 |
MOD_GSK3_1 | 200 | 207 | PF00069 | 0.658 |
MOD_GSK3_1 | 214 | 221 | PF00069 | 0.573 |
MOD_GSK3_1 | 223 | 230 | PF00069 | 0.676 |
MOD_GSK3_1 | 236 | 243 | PF00069 | 0.654 |
MOD_GSK3_1 | 245 | 252 | PF00069 | 0.553 |
MOD_GSK3_1 | 396 | 403 | PF00069 | 0.426 |
MOD_GSK3_1 | 427 | 434 | PF00069 | 0.581 |
MOD_GSK3_1 | 470 | 477 | PF00069 | 0.550 |
MOD_GSK3_1 | 479 | 486 | PF00069 | 0.505 |
MOD_GSK3_1 | 490 | 497 | PF00069 | 0.488 |
MOD_GSK3_1 | 509 | 516 | PF00069 | 0.636 |
MOD_GSK3_1 | 539 | 546 | PF00069 | 0.531 |
MOD_GSK3_1 | 70 | 77 | PF00069 | 0.442 |
MOD_N-GLC_1 | 218 | 223 | PF02516 | 0.585 |
MOD_N-GLC_1 | 236 | 241 | PF02516 | 0.605 |
MOD_NEK2_1 | 245 | 250 | PF00069 | 0.549 |
MOD_NEK2_1 | 341 | 346 | PF00069 | 0.462 |
MOD_NEK2_1 | 407 | 412 | PF00069 | 0.390 |
MOD_NEK2_1 | 490 | 495 | PF00069 | 0.537 |
MOD_NEK2_1 | 539 | 544 | PF00069 | 0.618 |
MOD_NEK2_1 | 70 | 75 | PF00069 | 0.419 |
MOD_NEK2_1 | 85 | 90 | PF00069 | 0.416 |
MOD_NEK2_2 | 400 | 405 | PF00069 | 0.441 |
MOD_NEK2_2 | 494 | 499 | PF00069 | 0.498 |
MOD_PIKK_1 | 261 | 267 | PF00454 | 0.435 |
MOD_PIKK_1 | 319 | 325 | PF00454 | 0.338 |
MOD_PIKK_1 | 499 | 505 | PF00454 | 0.770 |
MOD_PIKK_1 | 526 | 532 | PF00454 | 0.535 |
MOD_PKA_2 | 101 | 107 | PF00069 | 0.406 |
MOD_PKA_2 | 192 | 198 | PF00069 | 0.581 |
MOD_PKA_2 | 200 | 206 | PF00069 | 0.556 |
MOD_PKA_2 | 283 | 289 | PF00069 | 0.333 |
MOD_PKA_2 | 580 | 586 | PF00069 | 0.619 |
MOD_Plk_1 | 218 | 224 | PF00069 | 0.682 |
MOD_Plk_4 | 70 | 76 | PF00069 | 0.391 |
MOD_Plk_4 | 85 | 91 | PF00069 | 0.378 |
MOD_ProDKin_1 | 137 | 143 | PF00069 | 0.595 |
MOD_ProDKin_1 | 152 | 158 | PF00069 | 0.606 |
MOD_ProDKin_1 | 159 | 165 | PF00069 | 0.562 |
MOD_ProDKin_1 | 195 | 201 | PF00069 | 0.573 |
MOD_ProDKin_1 | 223 | 229 | PF00069 | 0.585 |
MOD_ProDKin_1 | 247 | 253 | PF00069 | 0.563 |
MOD_ProDKin_1 | 380 | 386 | PF00069 | 0.335 |
MOD_ProDKin_1 | 421 | 427 | PF00069 | 0.462 |
MOD_ProDKin_1 | 451 | 457 | PF00069 | 0.605 |
MOD_ProDKin_1 | 520 | 526 | PF00069 | 0.641 |
MOD_ProDKin_1 | 550 | 556 | PF00069 | 0.525 |
MOD_ProDKin_1 | 561 | 567 | PF00069 | 0.534 |
MOD_SUMO_rev_2 | 77 | 81 | PF00179 | 0.390 |
TRG_DiLeu_BaEn_1 | 267 | 272 | PF01217 | 0.409 |
TRG_ENDOCYTIC_2 | 180 | 183 | PF00928 | 0.594 |
TRG_ENDOCYTIC_2 | 268 | 271 | PF00928 | 0.409 |
TRG_ENDOCYTIC_2 | 362 | 365 | PF00928 | 0.540 |
TRG_ENDOCYTIC_2 | 373 | 376 | PF00928 | 0.268 |
TRG_ENDOCYTIC_2 | 401 | 404 | PF00928 | 0.353 |
TRG_ENDOCYTIC_2 | 501 | 504 | PF00928 | 0.553 |
TRG_ENDOCYTIC_2 | 514 | 517 | PF00928 | 0.550 |
TRG_ER_diArg_1 | 169 | 171 | PF00400 | 0.603 |
TRG_ER_diArg_1 | 258 | 260 | PF00400 | 0.457 |
TRG_Pf-PMV_PEXEL_1 | 174 | 178 | PF00026 | 0.564 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HV78 | Leptomonas seymouri | 51% | 94% |
A0A3R7KFH5 | Trypanosoma rangeli | 27% | 100% |
A4HDK3 | Leishmania braziliensis | 27% | 93% |
A4HDK4 | Leishmania braziliensis | 27% | 93% |
A4HS49 | Leishmania infantum | 99% | 100% |
E9AK36 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 100% |
O97201 | Leishmania major | 90% | 99% |
Q4QAJ3 | Leishmania major | 29% | 97% |
Q4QBX6 | Leishmania major | 22% | 100% |