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: 7 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005789 | endoplasmic reticulum membrane | 4 | 2 |
GO:0005886 | plasma membrane | 3 | 2 |
GO:0016020 | membrane | 2 | 2 |
GO:0031090 | organelle membrane | 3 | 2 |
GO:0044232 | organelle membrane contact site | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
GO:0140268 | endoplasmic reticulum-plasma membrane contact site | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 2 |
GO:0006869 | lipid transport | 5 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0015850 | organic hydroxy compound transport | 5 | 2 |
GO:0015918 | sterol transport | 6 | 2 |
GO:0032365 | intracellular lipid transport | 4 | 2 |
GO:0032366 | intracellular sterol transport | 5 | 2 |
GO:0046907 | intracellular transport | 3 | 2 |
GO:0051179 | localization | 1 | 2 |
GO:0051234 | establishment of localization | 2 | 2 |
GO:0051641 | cellular localization | 2 | 2 |
GO:0051649 | establishment of localization in cell | 3 | 2 |
GO:0071702 | organic substance transport | 4 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 2 |
GO:0005319 | lipid transporter activity | 2 | 2 |
GO:0005488 | binding | 1 | 2 |
GO:0005496 | steroid binding | 3 | 2 |
GO:0008289 | lipid binding | 2 | 2 |
GO:0015248 | sterol transporter activity | 3 | 2 |
GO:0032934 | sterol binding | 4 | 2 |
GO:0097159 | organic cyclic compound binding | 2 | 2 |
GO:0120013 | lipid transfer activity | 3 | 2 |
GO:0120015 | sterol transfer activity | 4 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 474 | 478 | PF00656 | 0.420 |
CLV_C14_Caspase3-7 | 521 | 525 | PF00656 | 0.497 |
CLV_C14_Caspase3-7 | 638 | 642 | PF00656 | 0.357 |
CLV_NRD_NRD_1 | 13 | 15 | PF00675 | 0.382 |
CLV_NRD_NRD_1 | 185 | 187 | PF00675 | 0.692 |
CLV_NRD_NRD_1 | 222 | 224 | PF00675 | 0.745 |
CLV_NRD_NRD_1 | 435 | 437 | PF00675 | 0.440 |
CLV_NRD_NRD_1 | 535 | 537 | PF00675 | 0.503 |
CLV_NRD_NRD_1 | 627 | 629 | PF00675 | 0.297 |
CLV_PCSK_FUR_1 | 533 | 537 | PF00082 | 0.501 |
CLV_PCSK_KEX2_1 | 13 | 15 | PF00082 | 0.382 |
CLV_PCSK_KEX2_1 | 185 | 187 | PF00082 | 0.698 |
CLV_PCSK_KEX2_1 | 221 | 223 | PF00082 | 0.674 |
CLV_PCSK_KEX2_1 | 435 | 437 | PF00082 | 0.440 |
CLV_PCSK_KEX2_1 | 535 | 537 | PF00082 | 0.503 |
CLV_PCSK_PC1ET2_1 | 221 | 223 | PF00082 | 0.570 |
CLV_PCSK_SKI1_1 | 134 | 138 | PF00082 | 0.522 |
CLV_PCSK_SKI1_1 | 225 | 229 | PF00082 | 0.635 |
CLV_PCSK_SKI1_1 | 293 | 297 | PF00082 | 0.651 |
CLV_PCSK_SKI1_1 | 545 | 549 | PF00082 | 0.777 |
CLV_PCSK_SKI1_1 | 650 | 654 | PF00082 | 0.258 |
CLV_PCSK_SKI1_1 | 690 | 694 | PF00082 | 0.312 |
DEG_COP1_1 | 156 | 166 | PF00400 | 0.554 |
DEG_SPOP_SBC_1 | 143 | 147 | PF00917 | 0.541 |
DEG_SPOP_SBC_1 | 239 | 243 | PF00917 | 0.588 |
DOC_CKS1_1 | 659 | 664 | PF01111 | 0.297 |
DOC_CYCLIN_yCln2_LP_2 | 595 | 601 | PF00134 | 0.582 |
DOC_MAPK_DCC_7 | 315 | 323 | PF00069 | 0.380 |
DOC_MAPK_gen_1 | 4 | 11 | PF00069 | 0.465 |
DOC_MAPK_MEF2A_6 | 315 | 323 | PF00069 | 0.369 |
DOC_PP1_RVXF_1 | 543 | 550 | PF00149 | 0.615 |
DOC_PP2B_LxvP_1 | 595 | 598 | PF13499 | 0.571 |
DOC_PP4_FxxP_1 | 402 | 405 | PF00568 | 0.403 |
DOC_PP4_FxxP_1 | 560 | 563 | PF00568 | 0.632 |
DOC_PP4_FxxP_1 | 659 | 662 | PF00568 | 0.339 |
DOC_USP7_MATH_1 | 153 | 157 | PF00917 | 0.642 |
DOC_USP7_MATH_1 | 176 | 180 | PF00917 | 0.834 |
DOC_USP7_MATH_1 | 233 | 237 | PF00917 | 0.719 |
DOC_USP7_MATH_1 | 240 | 244 | PF00917 | 0.748 |
DOC_USP7_MATH_1 | 274 | 278 | PF00917 | 0.614 |
DOC_USP7_MATH_1 | 34 | 38 | PF00917 | 0.553 |
DOC_USP7_MATH_1 | 529 | 533 | PF00917 | 0.518 |
DOC_USP7_MATH_1 | 56 | 60 | PF00917 | 0.523 |
DOC_USP7_MATH_1 | 723 | 727 | PF00917 | 0.371 |
DOC_USP7_UBL2_3 | 220 | 224 | PF12436 | 0.635 |
DOC_USP7_UBL2_3 | 684 | 688 | PF12436 | 0.357 |
DOC_WW_Pin1_4 | 155 | 160 | PF00397 | 0.644 |
DOC_WW_Pin1_4 | 303 | 308 | PF00397 | 0.600 |
DOC_WW_Pin1_4 | 4 | 9 | PF00397 | 0.546 |
DOC_WW_Pin1_4 | 401 | 406 | PF00397 | 0.420 |
DOC_WW_Pin1_4 | 448 | 453 | PF00397 | 0.382 |
DOC_WW_Pin1_4 | 658 | 663 | PF00397 | 0.297 |
LIG_14-3-3_CanoR_1 | 27 | 36 | PF00244 | 0.527 |
LIG_14-3-3_CanoR_1 | 435 | 441 | PF00244 | 0.393 |
LIG_14-3-3_CanoR_1 | 628 | 632 | PF00244 | 0.299 |
LIG_14-3-3_CanoR_1 | 63 | 67 | PF00244 | 0.421 |
LIG_Actin_WH2_2 | 26 | 43 | PF00022 | 0.502 |
LIG_AP2alpha_2 | 400 | 402 | PF02296 | 0.477 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.628 |
LIG_BIR_III_4 | 329 | 333 | PF00653 | 0.446 |
LIG_BIR_III_4 | 611 | 615 | PF00653 | 0.508 |
LIG_eIF4E_1 | 438 | 444 | PF01652 | 0.360 |
LIG_FHA_1 | 158 | 164 | PF00498 | 0.557 |
LIG_FHA_1 | 24 | 30 | PF00498 | 0.462 |
LIG_FHA_1 | 322 | 328 | PF00498 | 0.514 |
LIG_FHA_1 | 355 | 361 | PF00498 | 0.404 |
LIG_FHA_1 | 451 | 457 | PF00498 | 0.407 |
LIG_FHA_1 | 484 | 490 | PF00498 | 0.430 |
LIG_FHA_1 | 493 | 499 | PF00498 | 0.555 |
LIG_FHA_1 | 50 | 56 | PF00498 | 0.675 |
LIG_FHA_1 | 515 | 521 | PF00498 | 0.450 |
LIG_FHA_1 | 549 | 555 | PF00498 | 0.597 |
LIG_FHA_1 | 614 | 620 | PF00498 | 0.550 |
LIG_FHA_1 | 706 | 712 | PF00498 | 0.362 |
LIG_FHA_2 | 229 | 235 | PF00498 | 0.655 |
LIG_FHA_2 | 265 | 271 | PF00498 | 0.546 |
LIG_FHA_2 | 304 | 310 | PF00498 | 0.536 |
LIG_FHA_2 | 324 | 330 | PF00498 | 0.512 |
LIG_FHA_2 | 348 | 354 | PF00498 | 0.454 |
LIG_FHA_2 | 381 | 387 | PF00498 | 0.467 |
LIG_FHA_2 | 472 | 478 | PF00498 | 0.416 |
LIG_FHA_2 | 5 | 11 | PF00498 | 0.516 |
LIG_FHA_2 | 539 | 545 | PF00498 | 0.486 |
LIG_FHA_2 | 636 | 642 | PF00498 | 0.357 |
LIG_LIR_Apic_2 | 348 | 354 | PF02991 | 0.536 |
LIG_LIR_Apic_2 | 400 | 405 | PF02991 | 0.413 |
LIG_LIR_Apic_2 | 557 | 563 | PF02991 | 0.624 |
LIG_LIR_Gen_1 | 317 | 327 | PF02991 | 0.409 |
LIG_LIR_Gen_1 | 356 | 365 | PF02991 | 0.361 |
LIG_LIR_Gen_1 | 439 | 448 | PF02991 | 0.399 |
LIG_LIR_Gen_1 | 481 | 489 | PF02991 | 0.433 |
LIG_LIR_Gen_1 | 517 | 527 | PF02991 | 0.444 |
LIG_LIR_Gen_1 | 661 | 672 | PF02991 | 0.314 |
LIG_LIR_Gen_1 | 677 | 687 | PF02991 | 0.227 |
LIG_LIR_Gen_1 | 718 | 729 | PF02991 | 0.298 |
LIG_LIR_Nem_3 | 248 | 254 | PF02991 | 0.644 |
LIG_LIR_Nem_3 | 317 | 323 | PF02991 | 0.400 |
LIG_LIR_Nem_3 | 356 | 362 | PF02991 | 0.360 |
LIG_LIR_Nem_3 | 367 | 373 | PF02991 | 0.322 |
LIG_LIR_Nem_3 | 439 | 444 | PF02991 | 0.359 |
LIG_LIR_Nem_3 | 481 | 485 | PF02991 | 0.430 |
LIG_LIR_Nem_3 | 517 | 522 | PF02991 | 0.436 |
LIG_LIR_Nem_3 | 630 | 634 | PF02991 | 0.282 |
LIG_LIR_Nem_3 | 661 | 667 | PF02991 | 0.314 |
LIG_LIR_Nem_3 | 677 | 683 | PF02991 | 0.298 |
LIG_LIR_Nem_3 | 718 | 724 | PF02991 | 0.357 |
LIG_PCNA_yPIPBox_3 | 352 | 364 | PF02747 | 0.452 |
LIG_Pex14_2 | 104 | 108 | PF04695 | 0.484 |
LIG_Pex14_2 | 627 | 631 | PF04695 | 0.298 |
LIG_Pex14_2 | 643 | 647 | PF04695 | 0.298 |
LIG_Pex14_2 | 710 | 714 | PF04695 | 0.298 |
LIG_REV1ctd_RIR_1 | 135 | 143 | PF16727 | 0.553 |
LIG_SH2_CRK | 721 | 725 | PF00017 | 0.346 |
LIG_SH2_NCK_1 | 116 | 120 | PF00017 | 0.458 |
LIG_SH2_NCK_1 | 441 | 445 | PF00017 | 0.412 |
LIG_SH2_PTP2 | 359 | 362 | PF00017 | 0.348 |
LIG_SH2_SRC | 680 | 683 | PF00017 | 0.357 |
LIG_SH2_STAP1 | 209 | 213 | PF00017 | 0.645 |
LIG_SH2_STAP1 | 438 | 442 | PF00017 | 0.363 |
LIG_SH2_STAP1 | 721 | 725 | PF00017 | 0.287 |
LIG_SH2_STAT5 | 320 | 323 | PF00017 | 0.398 |
LIG_SH2_STAT5 | 359 | 362 | PF00017 | 0.348 |
LIG_SH2_STAT5 | 370 | 373 | PF00017 | 0.330 |
LIG_SH2_STAT5 | 376 | 379 | PF00017 | 0.383 |
LIG_SH2_STAT5 | 438 | 441 | PF00017 | 0.365 |
LIG_SH2_STAT5 | 657 | 660 | PF00017 | 0.357 |
LIG_SH3_2 | 284 | 289 | PF14604 | 0.699 |
LIG_SH3_3 | 199 | 205 | PF00018 | 0.601 |
LIG_SH3_3 | 281 | 287 | PF00018 | 0.714 |
LIG_SH3_3 | 544 | 550 | PF00018 | 0.544 |
LIG_SUMO_SIM_anti_2 | 30 | 37 | PF11976 | 0.516 |
LIG_SUMO_SIM_par_1 | 471 | 477 | PF11976 | 0.423 |
LIG_TRAF2_1 | 550 | 553 | PF00917 | 0.600 |
LIG_TRAF2_2 | 202 | 207 | PF00917 | 0.553 |
LIG_TRAF2_2 | 550 | 555 | PF00917 | 0.500 |
LIG_TYR_ITIM | 678 | 683 | PF00017 | 0.371 |
LIG_TYR_ITSM | 437 | 444 | PF00017 | 0.419 |
LIG_WRC_WIRS_1 | 105 | 110 | PF05994 | 0.495 |
LIG_WRC_WIRS_1 | 506 | 511 | PF05994 | 0.447 |
LIG_WRC_WIRS_1 | 640 | 645 | PF05994 | 0.357 |
LIG_WW_3 | 446 | 450 | PF00397 | 0.527 |
MOD_CK1_1 | 142 | 148 | PF00069 | 0.631 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.535 |
MOD_CK1_1 | 23 | 29 | PF00069 | 0.458 |
MOD_CK1_1 | 257 | 263 | PF00069 | 0.709 |
MOD_CK1_1 | 291 | 297 | PF00069 | 0.695 |
MOD_CK1_1 | 344 | 350 | PF00069 | 0.452 |
MOD_CK1_1 | 380 | 386 | PF00069 | 0.561 |
MOD_CK1_1 | 59 | 65 | PF00069 | 0.494 |
MOD_CK2_1 | 228 | 234 | PF00069 | 0.681 |
MOD_CK2_1 | 322 | 328 | PF00069 | 0.508 |
MOD_CK2_1 | 347 | 353 | PF00069 | 0.459 |
MOD_CK2_1 | 4 | 10 | PF00069 | 0.531 |
MOD_CK2_1 | 520 | 526 | PF00069 | 0.472 |
MOD_CK2_1 | 71 | 77 | PF00069 | 0.534 |
MOD_Cter_Amidation | 183 | 186 | PF01082 | 0.675 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.596 |
MOD_GlcNHglycan | 211 | 214 | PF01048 | 0.842 |
MOD_GlcNHglycan | 234 | 238 | PF01048 | 0.662 |
MOD_GlcNHglycan | 262 | 265 | PF01048 | 0.644 |
MOD_GlcNHglycan | 276 | 279 | PF01048 | 0.628 |
MOD_GlcNHglycan | 379 | 382 | PF01048 | 0.472 |
MOD_GlcNHglycan | 511 | 514 | PF01048 | 0.567 |
MOD_GlcNHglycan | 649 | 653 | PF01048 | 0.333 |
MOD_GlcNHglycan | 721 | 724 | PF01048 | 0.325 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.478 |
MOD_GSK3_1 | 139 | 146 | PF00069 | 0.575 |
MOD_GSK3_1 | 147 | 154 | PF00069 | 0.581 |
MOD_GSK3_1 | 172 | 179 | PF00069 | 0.685 |
MOD_GSK3_1 | 23 | 30 | PF00069 | 0.430 |
MOD_GSK3_1 | 235 | 242 | PF00069 | 0.739 |
MOD_GSK3_1 | 256 | 263 | PF00069 | 0.709 |
MOD_GSK3_1 | 274 | 281 | PF00069 | 0.617 |
MOD_GSK3_1 | 341 | 348 | PF00069 | 0.431 |
MOD_GSK3_1 | 45 | 52 | PF00069 | 0.642 |
MOD_GSK3_1 | 488 | 495 | PF00069 | 0.435 |
MOD_GSK3_1 | 505 | 512 | PF00069 | 0.440 |
MOD_GSK3_1 | 55 | 62 | PF00069 | 0.482 |
MOD_GSK3_1 | 635 | 642 | PF00069 | 0.357 |
MOD_GSK3_1 | 67 | 74 | PF00069 | 0.534 |
MOD_GSK3_1 | 705 | 712 | PF00069 | 0.298 |
MOD_GSK3_1 | 719 | 726 | PF00069 | 0.298 |
MOD_LATS_1 | 25 | 31 | PF00433 | 0.505 |
MOD_N-GLC_1 | 20 | 25 | PF02516 | 0.455 |
MOD_N-GLC_1 | 289 | 294 | PF02516 | 0.644 |
MOD_N-GLC_1 | 344 | 349 | PF02516 | 0.390 |
MOD_N-GLC_1 | 70 | 75 | PF02516 | 0.416 |
MOD_N-GLC_1 | 705 | 710 | PF02516 | 0.357 |
MOD_NEK2_1 | 104 | 109 | PF00069 | 0.488 |
MOD_NEK2_1 | 141 | 146 | PF00069 | 0.591 |
MOD_NEK2_1 | 321 | 326 | PF00069 | 0.461 |
MOD_NEK2_1 | 507 | 512 | PF00069 | 0.452 |
MOD_NEK2_1 | 514 | 519 | PF00069 | 0.462 |
MOD_NEK2_1 | 554 | 559 | PF00069 | 0.566 |
MOD_NEK2_1 | 610 | 615 | PF00069 | 0.522 |
MOD_NEK2_1 | 627 | 632 | PF00069 | 0.298 |
MOD_NEK2_1 | 639 | 644 | PF00069 | 0.304 |
MOD_NEK2_1 | 667 | 672 | PF00069 | 0.400 |
MOD_NEK2_1 | 705 | 710 | PF00069 | 0.298 |
MOD_OFUCOSY | 69 | 75 | PF10250 | 0.483 |
MOD_PIKK_1 | 107 | 113 | PF00454 | 0.479 |
MOD_PIKK_1 | 245 | 251 | PF00454 | 0.677 |
MOD_PIKK_1 | 254 | 260 | PF00454 | 0.545 |
MOD_PIKK_1 | 34 | 40 | PF00454 | 0.559 |
MOD_PIKK_1 | 380 | 386 | PF00454 | 0.477 |
MOD_PIKK_1 | 497 | 503 | PF00454 | 0.465 |
MOD_PIKK_1 | 548 | 554 | PF00454 | 0.494 |
MOD_PIKK_1 | 723 | 729 | PF00454 | 0.371 |
MOD_PK_1 | 139 | 145 | PF00069 | 0.543 |
MOD_PK_1 | 688 | 694 | PF00069 | 0.371 |
MOD_PKA_1 | 225 | 231 | PF00069 | 0.795 |
MOD_PKA_2 | 483 | 489 | PF00069 | 0.555 |
MOD_PKA_2 | 62 | 68 | PF00069 | 0.412 |
MOD_PKA_2 | 627 | 633 | PF00069 | 0.299 |
MOD_Plk_1 | 139 | 145 | PF00069 | 0.543 |
MOD_Plk_1 | 264 | 270 | PF00069 | 0.615 |
MOD_Plk_1 | 344 | 350 | PF00069 | 0.395 |
MOD_Plk_1 | 415 | 421 | PF00069 | 0.460 |
MOD_Plk_1 | 554 | 560 | PF00069 | 0.486 |
MOD_Plk_1 | 59 | 65 | PF00069 | 0.596 |
MOD_Plk_1 | 648 | 654 | PF00069 | 0.296 |
MOD_Plk_1 | 705 | 711 | PF00069 | 0.357 |
MOD_Plk_4 | 104 | 110 | PF00069 | 0.473 |
MOD_Plk_4 | 354 | 360 | PF00069 | 0.415 |
MOD_Plk_4 | 436 | 442 | PF00069 | 0.367 |
MOD_Plk_4 | 471 | 477 | PF00069 | 0.512 |
MOD_Plk_4 | 635 | 641 | PF00069 | 0.307 |
MOD_Plk_4 | 705 | 711 | PF00069 | 0.298 |
MOD_ProDKin_1 | 155 | 161 | PF00069 | 0.644 |
MOD_ProDKin_1 | 303 | 309 | PF00069 | 0.593 |
MOD_ProDKin_1 | 4 | 10 | PF00069 | 0.537 |
MOD_ProDKin_1 | 401 | 407 | PF00069 | 0.421 |
MOD_ProDKin_1 | 448 | 454 | PF00069 | 0.369 |
MOD_ProDKin_1 | 658 | 664 | PF00069 | 0.297 |
MOD_SUMO_rev_2 | 677 | 686 | PF00179 | 0.357 |
MOD_SUMO_rev_2 | 696 | 703 | PF00179 | 0.357 |
TRG_DiLeu_BaEn_1 | 317 | 322 | PF01217 | 0.399 |
TRG_DiLeu_BaEn_1 | 97 | 102 | PF01217 | 0.530 |
TRG_DiLeu_BaEn_4 | 97 | 103 | PF01217 | 0.395 |
TRG_DiLeu_BaLyEn_6 | 96 | 101 | PF01217 | 0.489 |
TRG_ENDOCYTIC_2 | 116 | 119 | PF00928 | 0.436 |
TRG_ENDOCYTIC_2 | 320 | 323 | PF00928 | 0.398 |
TRG_ENDOCYTIC_2 | 359 | 362 | PF00928 | 0.348 |
TRG_ENDOCYTIC_2 | 441 | 444 | PF00928 | 0.354 |
TRG_ENDOCYTIC_2 | 657 | 660 | PF00928 | 0.357 |
TRG_ENDOCYTIC_2 | 680 | 683 | PF00928 | 0.357 |
TRG_ENDOCYTIC_2 | 721 | 724 | PF00928 | 0.287 |
TRG_ER_diArg_1 | 13 | 15 | PF00400 | 0.382 |
TRG_ER_diArg_1 | 435 | 437 | PF00400 | 0.440 |
TRG_ER_diArg_1 | 533 | 536 | PF00400 | 0.503 |
TRG_NLS_MonoCore_2 | 219 | 224 | PF00514 | 0.659 |
TRG_NLS_MonoExtC_3 | 219 | 224 | PF00514 | 0.689 |
TRG_NLS_MonoExtN_4 | 219 | 225 | PF00514 | 0.620 |
TRG_NLS_MonoExtN_4 | 533 | 540 | PF00514 | 0.509 |
TRG_Pf-PMV_PEXEL_1 | 27 | 31 | PF00026 | 0.508 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I443 | Leptomonas seymouri | 56% | 100% |
A0A3R7L2R2 | Trypanosoma rangeli | 36% | 100% |
A0A3S7X3S1 | Leishmania donovani | 90% | 100% |
A4HIK4 | Leishmania braziliensis | 69% | 100% |
A4I5U9 | Leishmania infantum | 90% | 100% |
E9B144 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |